Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 80012 |
|---|---|
| ensemblid | ENSG00000173889.16 |
| hgncid | 15682 |
| symbol | PHC3 |
| name | polyhomeotic homolog 3 |
| refseq_nuc | NM_024947.4 |
| refseq_prot | NP_079223.3 |
| ensembl_nuc | ENST00000495893.7 |
| ensembl_prot | ENSP00000420294.1 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 170087584 |
| end | 170181733 |
| strand | - |
| ver | v1.2 |
| region | chr3:170087584-170181733 |
| region5000 | chr3:170082584-170186733 |
| regionname0 | PHC3_chr3_170087584_170181733 |
| regionname5000 | PHC3_chr3_170082584_170186733 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 995 | 319 | 71 | 63 | 147 | 14 | 22 | 106 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0002 | 0/0 | 995 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0003 | 0/0 | 995 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0004 | 0/0 | 995 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0005 | 0/0 | 995 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0006 | 0/0 | 995 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0007 | 0/0 | 995 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0008 | 0/0 | 995 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0009 | 0/0 | 995 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0010 | 0/0 | 995 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0011 | 0/0 | 995 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2988 | 296 | 67 | 63 | 129 | 14 | 21 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| c0002 | 0/0 | 2988 | 18 | 0 | 0 | 17 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| c0003 | 0/0 | 2988 | 4 | 4 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| c0004 | 0/0 | 2988 | 3 | 3 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| c0005 | 0/0 | 2988 | 2 | 1 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| c0006 | 0/0 | 2988 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| c0007 | 0/0 | 2988 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| c0008 | 0/0 | 2988 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| c0009 | 0/0 | 2988 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| c0010 | 0/0 | 2988 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| c0011 | 0/0 | 2988 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| c0012 | 0/0 | 2988 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| c0013 | 0/0 | 2988 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| c0014 | 0/0 | 2988 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 9662 | 73 | 5 | 17 | 40 | 6 | 5 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0002 | 0/0 | 9665 | 57 | 1 | 8 | 35 | 5 | 8 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0003 | 1/0 | 9665 | 36 | 13 | 8 | 11 | 1 | 2 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0004 | 0/1 | 9664 | 32 | 3 | 5 | 23 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0005 | 0/0 | 9665 | 16 | 0 | 0 | 16 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0006 | 0/0 | 9665 | 11 | 11 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0007 | 0/0 | 9664 | 10 | 1 | 7 | 2 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0008 | 0/0 | 9665 | 8 | 8 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0009 | 0/0 | 9662 | 8 | 1 | 3 | 0 | 1 | 3 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0010 | 0/0 | 9662 | 6 | 2 | 1 | 2 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0011 | 0/0 | 9662 | 5 | 0 | 0 | 5 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0012 | 0/0 | 9663 | 4 | 2 | 2 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0013 | 0/0 | 9662 | 3 | 0 | 3 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0014 | 0/0 | 9663 | 3 | 3 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0015 | 0/0 | 9665 | 3 | 3 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0016 | 0/0 | 9665 | 3 | 3 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0017 | 0/0 | 9666 | 3 | 3 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0018 | 0/0 | 9664 | 3 | 3 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0019 | 0/0 | 9665 | 3 | 2 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0020 | 0/0 | 9662 | 2 | 0 | 2 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0021 | 0/0 | 9662 | 2 | 0 | 0 | 0 | 0 | 2 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0022 | 0/0 | 9665 | 2 | 0 | 2 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0023 | 0/0 | 9665 | 2 | 1 | 0 | 0 | 1 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0024 | 0/0 | 9665 | 2 | 0 | 0 | 1 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0025 | 0/0 | 9666 | 2 | 2 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0026 | 0/0 | 9665 | 2 | 0 | 0 | 2 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0027 | 0/0 | 9670 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0028 | 0/0 | 9670 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0029 | 0/0 | 9670 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0030 | 0/0 | 9662 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0031 | 0/0 | 9662 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0032 | 0/0 | 9662 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0033 | 0/0 | 9665 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0034 | 0/0 | 9662 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0035 | 0/0 | 9662 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0036 | 0/0 | 9665 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0037 | 0/0 | 9662 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0038 | 0/0 | 9662 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0039 | 0/0 | 9662 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0040 | 0/0 | 9662 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0041 | 0/0 | 9665 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0042 | 0/0 | 9663 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0043 | 0/0 | 9662 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0044 | 0/0 | 9665 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0045 | 0/0 | 9663 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0046 | 0/0 | 9665 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0047 | 0/0 | 9665 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0048 | 0/0 | 9665 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0049 | 0/0 | 9665 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0050 | 0/0 | 9665 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0051 | 0/0 | 9665 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0052 | 0/0 | 9665 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0053 | 0/0 | 9665 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0054 | 0/0 | 9663 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0055 | 0/0 | 9665 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0056 | 0/0 | 9664 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| t0057 | 0/0 | 9664 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0144 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0198 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2988 | 296 | 67 | 63 | 129 | 14 | 21 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0002 | 0/0 | 2988 | 18 | 0 | 0 | 17 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0003 | 0/0 | 2988 | 4 | 4 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0013 | 0/0 | 2988 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0002c0004 | 0/0 | 2988 | 3 | 3 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0003c0005 | 0/0 | 2988 | 2 | 1 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0004c0012 | 0/0 | 2988 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0005c0011 | 0/0 | 2988 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0006c0008 | 0/0 | 2988 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0007c0009 | 0/0 | 2988 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0008c0014 | 0/0 | 2988 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0009c0010 | 0/0 | 2988 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0010c0007 | 0/0 | 2988 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0011c0006 | 0/0 | 2988 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 12649 | 71 | 4 | 17 | 40 | 6 | 4 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0001t0002 | 0/0 | 12652 | 54 | 1 | 8 | 33 | 5 | 7 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0001t0003 | 1/0 | 12652 | 36 | 13 | 8 | 11 | 1 | 2 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0001t0004 | 0/1 | 12651 | 31 | 3 | 5 | 22 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0001t0006 | 0/0 | 12652 | 7 | 7 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0001t0007 | 0/0 | 12651 | 10 | 1 | 7 | 2 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0001t0008 | 0/0 | 12652 | 8 | 8 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0001t0009 | 0/0 | 12649 | 8 | 1 | 3 | 0 | 1 | 3 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0001t0010 | 0/0 | 12649 | 6 | 2 | 1 | 2 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0001t0011 | 0/0 | 12649 | 5 | 0 | 0 | 5 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0001t0012 | 0/0 | 12650 | 4 | 2 | 2 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0001t0013 | 0/0 | 12649 | 3 | 0 | 3 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0001t0014 | 0/0 | 12650 | 3 | 3 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0001t0015 | 0/0 | 12652 | 3 | 3 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0001t0016 | 0/0 | 12652 | 3 | 3 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0001t0018 | 0/0 | 12651 | 2 | 2 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0001t0019 | 0/0 | 12652 | 3 | 2 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0001t0020 | 0/0 | 12649 | 2 | 0 | 2 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0001t0021 | 0/0 | 12649 | 2 | 0 | 0 | 0 | 0 | 2 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0001t0022 | 0/0 | 12652 | 2 | 0 | 2 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0001t0023 | 0/0 | 12652 | 2 | 1 | 0 | 0 | 1 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0001t0025 | 0/0 | 12653 | 2 | 2 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0001t0026 | 0/0 | 12652 | 2 | 0 | 0 | 2 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0001t0030 | 0/0 | 12649 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0001t0031 | 0/0 | 12649 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0001t0032 | 0/0 | 12649 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0001t0033 | 0/0 | 12652 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0001t0034 | 0/0 | 12649 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0001t0035 | 0/0 | 12649 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0001t0036 | 0/0 | 12652 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0001t0037 | 0/0 | 12649 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0001t0038 | 0/0 | 12649 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0001t0039 | 0/0 | 12649 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0001t0040 | 0/0 | 12649 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0001t0041 | 0/0 | 12652 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0001t0042 | 0/0 | 12650 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0001t0043 | 0/0 | 12649 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0001t0045 | 0/0 | 12650 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0001t0046 | 0/0 | 12652 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0001t0047 | 0/0 | 12652 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0001t0048 | 0/0 | 12652 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0001t0049 | 0/0 | 12652 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0001t0050 | 0/0 | 12652 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0001t0051 | 0/0 | 12652 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0001t0052 | 0/0 | 12652 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0001t0053 | 0/0 | 12652 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0001t0054 | 0/0 | 12650 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0001t0055 | 0/0 | 12652 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0001t0056 | 0/0 | 12651 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0001t0057 | 0/0 | 12651 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0002t0005 | 0/0 | 12652 | 15 | 0 | 0 | 15 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0002t0024 | 0/0 | 12652 | 2 | 0 | 0 | 1 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0002t0044 | 0/0 | 12652 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0003t0006 | 0/0 | 12652 | 4 | 4 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0001c0013t0002 | 0/0 | 12652 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0002c0004t0017 | 0/0 | 12653 | 3 | 3 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0003c0005t0027 | 0/0 | 12657 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0003c0005t0028 | 0/0 | 12657 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0004c0012t0004 | 0/0 | 12651 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0005c0011t0002 | 0/0 | 12652 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0006c0008t0018 | 0/0 | 12651 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0007c0009t0001 | 0/0 | 12649 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0008c0014t0005 | 0/0 | 12652 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0009c0010t0001 | 0/0 | 12649 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0010c0007t0029 | 0/0 | 12657 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| a0011c0006t0002 | 0/0 | 12652 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | copy fasta | chr3 | 170082584 | 170186733 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0198 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0003g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0144 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0004g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0006g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0006g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0006g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0006g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0006g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0006g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0006g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0007g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0007g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0007g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0007g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0007g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0007g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0007g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0007g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0007g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0008g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0008g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0008g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0008g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0008g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0008g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0008g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0008g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0009g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0009g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0009g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0009g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0009g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0009g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0009g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0010g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0010g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0010g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0010g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0010g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0010g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0011g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0011g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0011g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0011g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0011g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0012g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0012g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0012g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0012g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0013g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0013g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0013g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0014g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0014g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0014g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0015g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0015g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0015g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0016g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0016g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0016g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0018g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0018g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0019g0001 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0020g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0020g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0021g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0021g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0022g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0022g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0023g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0023g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0025g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0025g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0026g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0026g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0030g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0031g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0032g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0033g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0034g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0035g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0036g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0037g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0038g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0039g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0040g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0041g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0042g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0043g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0045g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0046g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0047g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0048g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0049g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0050g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0051g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0052g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0053g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0054g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0055g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0056g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0001t0057g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0002t0005g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0002t0005g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0002t0005g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0002t0005g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0002t0005g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0002t0005g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0002t0005g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0002t0005g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0002t0005g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0002t0005g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0002t0005g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0002t0005g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0002t0005g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0002t0005g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0002t0005g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0002t0024g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0002t0024g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0002t0044g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0003t0006g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0003t0006g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0003t0006g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0003t0006g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0001c0013t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0002c0004t0017g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0002c0004t0017g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0002c0004t0017g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0003c0005t0027g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0003c0005t0028g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0004c0012t0004g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0005c0011t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0006c0008t0018g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0007c0009t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0008c0014t0005g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0009c0010t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0010c0007t0029g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| a0011c0006t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0227 | EUR | GBR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0216 | EUR | GBR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0078 | EUR | FIN | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0123 | EUR | FIN | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0094 | EUR | FIN | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0125 | EUR | FIN | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00408 | hp1 | a0001 | c0002 | t0005 | g0311 | EAS | CHS | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00423 | hp1 | a0001 | c0002 | t0005 | g0317 | EAS | CHS | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | CHS | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00438 | hp1 | a0001 | c0001 | t0011 | g0098 | EAS | CHS | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0197 | EAS | CHS | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | CHS | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00558 | hp1 | a0001 | c0002 | t0005 | g0314 | EAS | CHS | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00597 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | CHS | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00597 | hp2 | a0001 | c0001 | t0011 | g0291 | EAS | CHS | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | CHS | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00609 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | CHS | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00621 | hp1 | a0001 | c0001 | t0026 | g0274 | EAS | CHS | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00639 | hp1 | a0001 | c0001 | t0032 | g0115 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0145 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00642 | hp1 | a0001 | c0001 | t0035 | g0304 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00642 | hp2 | a0001 | c0001 | t0004 | g0136 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00673 | hp2 | a0001 | c0002 | t0005 | g0312 | EAS | CHS | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0200 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00735 | hp2 | a0001 | c0001 | t0050 | g0269 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00741 | hp1 | a0001 | c0001 | t0052 | g0243 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0283 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0146 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0228 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01109 | hp1 | a0001 | c0001 | t0009 | g0068 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01109 | hp2 | a0001 | c0001 | t0022 | g0234 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01167 | hp1 | a0001 | c0001 | t0012 | g0103 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01168 | hp1 | a0001 | c0001 | t0013 | g0008 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01168 | hp2 | a0001 | c0001 | t0020 | g0050 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01169 | hp1 | a0001 | c0001 | t0012 | g0102 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01169 | hp2 | a0001 | c0001 | t0020 | g0061 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0262 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01175 | hp2 | a0001 | c0001 | t0007 | g0126 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01192 | hp2 | a0001 | c0001 | t0013 | g0230 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01243 | hp1 | a0001 | c0001 | t0019 | g0001 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0199 | AMR | PUR | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01255 | hp2 | a0001 | c0001 | t0022 | g0007 | AMR | CLM | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0169 | AMR | CLM | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01257 | hp1 | a0001 | c0001 | t0007 | g0003 | AMR | CLM | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01257 | hp2 | a0001 | c0001 | t0009 | g0002 | AMR | CLM | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01258 | hp1 | a0001 | c0001 | t0009 | g0002 | AMR | CLM | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01258 | hp2 | a0001 | c0001 | t0004 | g0135 | AMR | CLM | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0231 | AMR | CLM | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0302 | AMR | CLM | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01346 | hp1 | a0001 | c0001 | t0007 | g0152 | AMR | CLM | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01346 | hp2 | a0001 | c0001 | t0013 | g0182 | AMR | CLM | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0267 | AMR | CLM | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01433 | hp1 | a0003 | c0005 | t0028 | g0325 | AMR | CLM | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01496 | hp1 | a0001 | c0001 | t0007 | g0003 | AMR | CLM | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0218 | AMR | CLM | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | IBS | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0124 | EUR | IBS | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0248 | EUR | IBS | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0279 | AFR | ACB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01884 | hp2 | a0001 | c0001 | t0016 | g0206 | AFR | ACB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0263 | AMR | PEL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0301 | AMR | PEL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01943 | hp1 | a0001 | c0001 | t0007 | g0195 | AMR | PEL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0219 | AMR | PEL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0303 | AMR | PEL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0181 | AMR | PEL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0299 | AMR | PEL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0224 | AMR | PEL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02004 | hp2 | a0001 | c0001 | t0007 | g0156 | AMR | PEL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02015 | hp1 | a0001 | c0002 | t0005 | g0310 | EAS | KHV | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | KHV | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02027 | hp2 | a0008 | c0014 | t0005 | g0321 | EAS | KHV | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0232 | EAS | KHV | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | KHV | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02055 | hp1 | a0003 | c0005 | t0027 | g0324 | AFR | ACB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02055 | hp2 | a0001 | c0001 | t0008 | g0327 | AFR | ACB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02056 | hp1 | a0001 | c0001 | t0004 | g0137 | EAS | KHV | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02071 | hp1 | a0001 | c0001 | t0004 | g0168 | EAS | KHV | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02071 | hp2 | a0001 | c0002 | t0024 | g0309 | EAS | KHV | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0202 | EAS | KHV | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | KHV | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | KHV | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02132 | hp1 | a0001 | c0001 | t0033 | g0239 | EAS | KHV | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02132 | hp2 | a0001 | c0001 | t0038 | g0024 | EAS | KHV | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | KHV | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0179 | AFR | ACB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0166 | AFR | ACB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0225 | AMR | PEL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0300 | AMR | PEL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02155 | hp1 | a0001 | c0002 | t0005 | g0320 | EAS | CDX | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | CDX | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02257 | hp1 | a0009 | c0010 | t0001 | g0107 | AFR | ACB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02257 | hp2 | a0001 | c0001 | t0014 | g0111 | AFR | ACB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02258 | hp1 | a0001 | c0001 | t0015 | g0256 | AFR | ACB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02258 | hp2 | a0001 | c0001 | t0016 | g0205 | AFR | ACB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02273 | hp2 | a0001 | c0001 | t0007 | g0171 | AMR | PEL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02280 | hp1 | a0001 | c0001 | t0009 | g0069 | AFR | ACB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0242 | AFR | ACB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0226 | AMR | PEL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0129 | AMR | PEL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02451 | hp1 | a0001 | c0001 | t0015 | g0254 | AFR | ACB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02451 | hp2 | a0001 | c0001 | t0031 | g0114 | AFR | ACB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02572 | hp2 | a0001 | c0001 | t0057 | g0187 | AFR | GWD | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02615 | hp1 | a0001 | c0001 | t0043 | g0030 | AFR | GWD | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02615 | hp2 | a0002 | c0004 | t0017 | g0196 | AFR | GWD | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02622 | hp1 | a0001 | c0001 | t0007 | g0149 | AFR | GWD | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02622 | hp2 | a0001 | c0001 | t0008 | g0117 | AFR | GWD | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02630 | hp1 | a0001 | c0001 | t0025 | g0253 | AFR | GWD | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02630 | hp2 | a0001 | c0001 | t0008 | g0175 | AFR | GWD | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0257 | AFR | GWD | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02717 | hp2 | a0001 | c0001 | t0010 | g0028 | AFR | GWD | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02809 | hp1 | a0001 | c0001 | t0006 | g0191 | AFR | GWD | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02809 | hp2 | a0001 | c0001 | t0015 | g0255 | AFR | GWD | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02818 | hp1 | a0001 | c0001 | t0045 | g0101 | AFR | GWD | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02818 | hp2 | a0001 | c0001 | t0008 | g0116 | AFR | GWD | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02886 | hp1 | a0001 | c0001 | t0041 | g0207 | AFR | GWD | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0264 | AFR | GWD | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02895 | hp1 | a0001 | c0001 | t0006 | g0280 | AFR | GWD | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02895 | hp2 | a0001 | c0001 | t0014 | g0110 | AFR | GWD | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02896 | hp1 | a0002 | c0004 | t0017 | g0063 | AFR | GWD | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02896 | hp2 | a0001 | c0001 | t0025 | g0292 | AFR | GWD | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02897 | hp1 | a0002 | c0004 | t0017 | g0062 | AFR | GWD | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02897 | hp2 | a0001 | c0001 | t0014 | g0109 | AFR | GWD | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02922 | hp1 | a0001 | c0001 | t0054 | g0105 | AFR | ESN | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02922 | hp2 | a0001 | c0001 | t0019 | g0001 | AFR | ESN | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02965 | hp1 | a0001 | c0001 | t0042 | g0194 | AFR | ESN | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0208 | AFR | ESN | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0211 | AFR | ESN | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02970 | hp2 | a0006 | c0008 | t0018 | g0150 | AFR | ESN | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02976 | hp1 | a0001 | c0001 | t0019 | g0001 | AFR | ESN | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02976 | hp2 | a0001 | c0003 | t0006 | g0295 | AFR | ESN | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03041 | hp1 | a0001 | c0001 | t0006 | g0189 | AFR | GWD | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03041 | hp2 | a0001 | c0001 | t0018 | g0170 | AFR | GWD | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03098 | hp1 | a0001 | c0001 | t0006 | g0141 | AFR | MSL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03098 | hp2 | a0001 | c0001 | t0018 | g0140 | AFR | MSL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0209 | AFR | ESN | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03139 | hp2 | a0001 | c0001 | t0008 | g0328 | AFR | ESN | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0266 | AFR | ESN | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03195 | hp2 | a0001 | c0001 | t0008 | g0176 | AFR | ESN | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03209 | hp1 | a0001 | c0001 | t0047 | g0212 | AFR | MSL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0174 | AFR | MSL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03239 | hp1 | a0001 | c0001 | t0021 | g0085 | SAS | PJL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0241 | SAS | PJL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0134 | AFR | MSL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03453 | hp2 | a0001 | c0003 | t0006 | g0294 | AFR | MSL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03486 | hp2 | a0001 | c0001 | t0006 | g0190 | AFR | MSL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03490 | hp1 | a0001 | c0001 | t0036 | g0071 | SAS | PJL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0223 | SAS | PJL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03492 | hp1 | a0001 | c0001 | t0009 | g0072 | SAS | PJL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03492 | hp2 | a0005 | c0011 | t0002 | g0237 | SAS | PJL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03579 | hp1 | a0001 | c0001 | t0008 | g0113 | AFR | MSL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0278 | SAS | STU | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03688 | hp2 | a0001 | c0001 | t0009 | g0064 | SAS | STU | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0298 | SAS | PJL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0265 | SAS | BEB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03831 | hp2 | a0001 | c0002 | t0024 | g0313 | SAS | BEB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03834 | hp1 | a0001 | c0001 | t0046 | g0277 | SAS | BEB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0281 | SAS | BEB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0131 | SAS | BEB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | BEB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG04184 | hp2 | a0001 | c0001 | t0021 | g0088 | SAS | BEB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG04199 | hp1 | a0007 | c0009 | t0001 | g0019 | SAS | STU | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | STU | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0183 | SAS | STU | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG04204 | hp2 | a0001 | c0001 | t0009 | g0067 | SAS | STU | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG04228 | hp1 | a0001 | c0001 | t0010 | g0020 | SAS | STU | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0215 | SAS | STU | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0159 | EAS | CHB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | CHB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | CHB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CHB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18940 | hp2 | a0001 | c0001 | t0004 | g0167 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18942 | hp2 | a0001 | c0001 | t0004 | g0148 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18943 | hp1 | a0001 | c0001 | t0004 | g0162 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18944 | hp1 | a0001 | c0001 | t0004 | g0151 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18946 | hp2 | a0001 | c0001 | t0040 | g0048 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18949 | hp2 | a0011 | c0006 | t0002 | g0122 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18950 | hp2 | a0001 | c0001 | t0004 | g0153 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18951 | hp2 | a0001 | c0002 | t0005 | g0326 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18957 | hp2 | a0001 | c0001 | t0004 | g0163 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0287 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18960 | hp1 | a0001 | c0001 | t0034 | g0089 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18960 | hp2 | a0001 | c0002 | t0005 | g0315 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18963 | hp2 | a0001 | c0001 | t0004 | g0127 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18964 | hp1 | a0001 | c0002 | t0005 | g0306 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18969 | hp2 | a0001 | c0001 | t0010 | g0095 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18975 | hp1 | a0001 | c0002 | t0005 | g0307 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18975 | hp2 | a0001 | c0001 | t0026 | g0238 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0268 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18982 | hp2 | a0001 | c0002 | t0005 | g0318 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18983 | hp1 | a0001 | c0001 | t0004 | g0155 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18983 | hp2 | a0001 | c0013 | t0002 | g0213 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18985 | hp1 | a0001 | c0002 | t0044 | g0316 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18985 | hp2 | a0001 | c0001 | t0004 | g0158 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18986 | hp1 | a0001 | c0001 | t0011 | g0076 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18986 | hp2 | a0001 | c0001 | t0049 | g0288 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18988 | hp2 | a0001 | c0001 | t0004 | g0154 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18991 | hp2 | a0001 | c0002 | t0005 | g0322 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18994 | hp1 | a0001 | c0001 | t0055 | g0138 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18994 | hp2 | a0001 | c0002 | t0005 | g0308 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18998 | hp2 | a0001 | c0001 | t0048 | g0297 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19003 | hp1 | a0001 | c0001 | t0056 | g0160 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19007 | hp1 | a0001 | c0001 | t0007 | g0143 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19010 | hp2 | a0001 | c0001 | t0004 | g0139 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19030 | hp1 | a0001 | c0001 | t0010 | g0029 | AFR | LWK | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19030 | hp2 | a0001 | c0001 | t0037 | g0099 | AFR | LWK | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19043 | hp1 | a0001 | c0003 | t0006 | g0296 | AFR | LWK | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19043 | hp2 | a0001 | c0001 | t0012 | g0100 | AFR | LWK | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19054 | hp1 | a0001 | c0001 | t0004 | g0161 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0157 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19063 | hp1 | a0001 | c0001 | t0053 | g0178 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19063 | hp2 | a0001 | c0001 | t0011 | g0087 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0233 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19066 | hp1 | a0001 | c0002 | t0005 | g0319 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19068 | hp1 | a0001 | c0001 | t0011 | g0065 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0204 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19076 | hp2 | a0001 | c0001 | t0004 | g0128 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19078 | hp1 | a0004 | c0012 | t0004 | g0173 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19082 | hp1 | a0001 | c0002 | t0005 | g0305 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19082 | hp2 | a0001 | c0001 | t0039 | g0009 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19085 | hp1 | a0001 | c0001 | t0010 | g0096 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19085 | hp2 | a0001 | c0001 | t0051 | g0245 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19086 | hp2 | a0001 | c0001 | t0004 | g0172 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19088 | hp2 | a0001 | c0001 | t0004 | g0164 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19091 | hp2 | a0001 | c0001 | t0004 | g0147 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19240 | hp1 | a0001 | c0001 | t0008 | g0177 | AFR | YRI | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0260 | AFR | YRI | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA20129 | hp1 | a0001 | c0001 | t0012 | g0104 | AFR | ASW | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA20129 | hp2 | a0001 | c0003 | t0006 | g0293 | AFR | ASW | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0240 | EUR | TSI | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA20752 | hp2 | a0001 | c0001 | t0009 | g0070 | EUR | TSI | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA20805 | hp1 | a0001 | c0001 | t0023 | g0220 | EUR | TSI | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0084 | EUR | TSI | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0217 | AMR | CLM | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG01123 | hp2 | a0001 | c0001 | t0010 | g0014 | AMR | CLM | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02109 | hp1 | a0001 | c0001 | t0006 | g0004 | AFR | ACB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02109 | hp2 | a0001 | c0001 | t0016 | g0282 | AFR | ACB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0261 | AFR | ACB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0165 | AFR | ACB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0259 | AFR | ACB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03471 | hp1 | a0010 | c0007 | t0029 | g0323 | AFR | MSL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0210 | AFR | MSL | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0258 | AFR | USA | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| HG06807 | hp2 | a0001 | c0001 | t0023 | g0221 | AFR | USA | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18955 | hp1 | a0001 | c0001 | t0030 | g0047 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| NA18955 | hp2 | a0001 | c0001 | t0007 | g0142 | EAS | JPT | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0004 | g0144 | REF | REF | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0198 | REF | REF | PHC3_chr3_170082584_170186733 | PHC3 | chr3 | 170082584 | 170186733 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:170113480
|
T | C | 1 | a0007 | 1 | HG04199.hp1 | missense_variant | MODERATE | c.2233A>G | p.Lys745Glu | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/15 | 2251/12652 | 2233/2988 | 745/995 | chr3 | 170113480 | ||
| chr3:170117321
|
T | C | 1 | a0008 | 1 | HG02027.hp2 | missense_variant | MODERATE | c.2098A>G | p.Ile700Val | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/15 | 2116/12652 | 2098/2988 | 700/995 | chr3 | 170117321 | ||
| chr3:170122683
|
C | T | 1 | a0006 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.1850G>A | p.Arg617Gln | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/15 | 1868/12652 | 1850/2988 | 617/995 | chr3 | 170122683 | ||
| chr3:170128979
|
T | C | 1 | a0009 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.1493A>G | p.His498Arg | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/15 | 1511/12652 | 1493/2988 | 498/995 | chr3 | 170128979 | ||
| chr3:170129100
|
C | G | 2 | a0003a0010 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
missense_variant | MODERATE | c.1372G>C | p.Ala458Pro | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/15 | 1390/12652 | 1372/2988 | 458/995 | chr3 | 170129100 | ||
| chr3:170129257
|
C | A | 1 | a0005 | 1 | HG03492.hp2 | missense_variant | MODERATE | c.1215G>T | p.Gln405His | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/15 | 1233/12652 | 1215/2988 | 405/995 | chr3 | 170129257 | ||
| chr3:170129294
|
G | A | 1 | a0004 | 1 | NA19078.hp1 | missense_variant | MODERATE | c.1178C>T | p.Pro393Leu | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/15 | 1196/12652 | 1178/2988 | 393/995 | chr3 | 170129294 | ||
| chr3:170129337
|
C | T | 1 | a0010 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.1135G>A | p.Ala379Thr | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/15 | 1153/12652 | 1135/2988 | 379/995 | chr3 | 170129337 | ||
| chr3:170171423
|
T | C | 1 | a0002 | 3 | HG02615.hp2 HG02896.hp1 HG02897.hp1 |
missense_variant | MODERATE | c.364A>G | p.Thr122Ala | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/15 | 382/12652 | 364/2988 | 122/995 | chr3 | 170171423 | ||
| chr3:170178790
|
C | T | 1 | a0011 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.163G>A | p.Asp55Asn | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/15 | 181/12652 | 163/2988 | 55/995 | chr3 | 170178790 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:170172686
|
G | A | 1 | a0001c0013 | 1 | NA18983.hp2 | synonymous_variant | LOW | c.207C>T | p.Pro69Pro | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 3/15 | 225/12652 | 207/2988 | 69/995 | chr3 | 170172686 | ||
| chr3:170178803
|
G | C | 2 | a0001c0002a0008c0014 | 19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
synonymous_variant | LOW | c.150C>G | p.Val50Val | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/15 | 168/12652 | 150/2988 | 50/995 | chr3 | 170178803 | ||
| chr3:170178896
|
C | T | 1 | a0001c0003 | 4 | HG02976.hp2 HG03453.hp2 NA19043.hp1 others(1): Show |
synonymous_variant | LOW | c.57G>A | p.Pro19Pro | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/15 | 75/12652 | 57/2988 | 19/995 | chr3 | 170178896 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:170087659
|
A | G | 1 | a0001c0001t0020 | 2 | HG01168.hp2 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9571T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 9571 | chr3 | 170087659 | |||||
| chr3:170087932
|
T | A | 1 | a0001c0002t0044 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9298A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 9298 | chr3 | 170087932 | |||||
| chr3:170088037
|
A | C | 1 | a0003c0005t0027 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9193T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 9193 | chr3 | 170088037 | |||||
| chr3:170088044
|
A | C | 1 | a0001c0001t0011 | 5 | HG00438.hp1 HG00597.hp2 NA18986.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*9186T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 9186 | chr3 | 170088044 | |||||
| chr3:170088121
|
T | C | 1 | a0001c0001t0038 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9109A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 9109 | chr3 | 170088121 | |||||
| chr3:170088189
|
G | C | 1 | a0001c0001t0039 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9041C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 9041 | chr3 | 170088189 | |||||
| chr3:170088283
|
T | C | 1 | a0001c0001t0021 | 2 | HG03239.hp1 HG04184.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8947A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 8947 | chr3 | 170088283 | |||||
| chr3:170088382
|
G | A | 7 | a0001c0001t0004a0001c0001t0007a0001c0001t0018others(4): Show | 47 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*8848C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 8848 | chr3 | 170088382 | |||||
| chr3:170088843
|
C | T | 1 | a0001c0001t0031 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8387G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 8387 | chr3 | 170088843 | |||||
| chr3:170088892
|
G | A | 1 | a0001c0001t0037 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8338C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 8338 | chr3 | 170088892 | |||||
| chr3:170089017
|
A | T | 1 | a0001c0001t0026 | 2 | HG00621.hp1 NA18975.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8213T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 8213 | chr3 | 170089017 | |||||
| chr3:170089028
|
A | G | 39 | a0001c0001t0001a0001c0001t0004a0001c0001t0007others(36): Show | 194 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(191): Show |
3_prime_UTR_variant | MODIFIER | c.*8202T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 8202 | chr3 | 170089028 | |||||
| chr3:170089109
|
T | C | 1 | a0001c0001t0046 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8121A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 8121 | chr3 | 170089109 | |||||
| chr3:170089188
|
A | G | 3 | a0003c0005t0027a0003c0005t0028a0010c0007t0029 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8042T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 8042 | chr3 | 170089188 | |||||
| chr3:170089442
|
T | C | 2 | a0001c0001t0009a0001c0001t0036 | 9 | HG01109.hp1 HG01257.hp2 HG01258.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*7788A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 7788 | chr3 | 170089442 | |||||
| chr3:170089627
|
A | G | 3 | a0003c0005t0027a0003c0005t0028a0010c0007t0029 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7603T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 7603 | chr3 | 170089627 | |||||
| chr3:170089635
|
G | A | 1 | a0001c0001t0008 | 8 | HG02055.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7595C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 7595 | chr3 | 170089635 | |||||
| chr3:170089745
|
C | T | 1 | a0001c0001t0049 | 1 | NA18986.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7485G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 7485 | chr3 | 170089745 | |||||
| chr3:170089836
|
C | G | 39 | a0001c0001t0001a0001c0001t0004a0001c0001t0007others(36): Show | 194 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(191): Show |
3_prime_UTR_variant | MODIFIER | c.*7394G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 7394 | chr3 | 170089836 | |||||
| chr3:170089863
|
G | A | 1 | a0001c0001t0040 | 1 | NA18946.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7367C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 7367 | chr3 | 170089863 | |||||
| chr3:170089927
|
A | G | 1 | a0001c0001t0037 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7303T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 7303 | chr3 | 170089927 | |||||
| chr3:170089927
|
AAG | A | 3 | a0001c0001t0012a0001c0001t0045a0001c0001t0054 | 6 | HG01167.hp1 HG01169.hp1 HG02818.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*7301_*7302delCT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 7301 | chr3 | 170089927 | |||||
| chr3:170089928
|
A | G | 2 | a0001c0001t0008a0001c0002t0044 | 9 | HG02055.hp2 HG02622.hp2 HG02630.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*7302T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 7302 | chr3 | 170089928 | |||||
| chr3:170089929
|
G | A | 3 | a0001c0001t0008a0001c0001t0047a0001c0002t0044 | 10 | HG02055.hp2 HG02622.hp2 HG02630.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*7301C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 7301 | chr3 | 170089929 | |||||
| chr3:170089929
|
G | GA | 6 | a0001c0001t0015a0001c0001t0019a0001c0001t0025others(3): Show | 13 | HG01243.hp1 HG02258.hp1 HG02451.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*7300dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 7300 | chr3 | 170089929 | |||||
| chr3:170089930
|
A | G | 3 | a0001c0001t0012a0001c0001t0045a0001c0001t0054 | 6 | HG01167.hp1 HG01169.hp1 HG02818.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*7300T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 7300 | chr3 | 170089930 | |||||
| chr3:170089972
|
G | C | 4 | a0001c0002t0005a0001c0002t0024a0001c0002t0044others(1): Show | 19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*7258C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 7258 | chr3 | 170089972 | |||||
| chr3:170090020
|
A | G | 1 | a0001c0001t0014 | 3 | HG02257.hp2 HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7210T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 7210 | chr3 | 170090020 | |||||
| chr3:170090051
|
G | T | 41 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(38): Show | 205 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(202): Show |
3_prime_UTR_variant | MODIFIER | c.*7179C>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 7179 | chr3 | 170090051 | |||||
| chr3:170090077
|
A | G | 3 | a0003c0005t0027a0003c0005t0028a0010c0007t0029 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7153T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 7153 | chr3 | 170090077 | |||||
| chr3:170090111
|
TA | T | 3 | a0001c0001t0015a0001c0001t0019a0001c0001t0057 | 7 | HG01243.hp1 HG02258.hp1 HG02451.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*7118delT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 7118 | chr3 | 170090111 | |||||
| chr3:170090130
|
A | G | 3 | a0001c0001t0012a0001c0001t0045a0001c0001t0054 | 6 | HG01167.hp1 HG01169.hp1 HG02818.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*7100T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 7100 | chr3 | 170090130 | |||||
| chr3:170090326
|
A | C | 12 | a0001c0001t0002a0001c0001t0023a0001c0001t0026others(9): Show | 67 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*6904T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 6904 | chr3 | 170090326 | |||||
| chr3:170090364
|
T | C | 2 | a0001c0001t0016a0002c0004t0017 | 6 | HG01884.hp2 HG02109.hp2 HG02258.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6866A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 6866 | chr3 | 170090364 | |||||
| chr3:170090417
|
AAT | A | 1 | a0001c0001t0014 | 3 | HG02257.hp2 HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6811_*6812delAT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 6811 | chr3 | 170090417 | |||||
| chr3:170090566
|
G | A | 7 | a0001c0001t0004a0001c0001t0007a0001c0001t0018others(4): Show | 47 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*6664C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 6664 | chr3 | 170090566 | |||||
| chr3:170090719
|
A | G | 1 | a0001c0001t0042 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6511T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 6511 | chr3 | 170090719 | |||||
| chr3:170091480
|
C | CCTCTT | 3 | a0003c0005t0027a0003c0005t0028a0010c0007t0029 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5749_*5750insAAGA others(1): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 5749 | chr3 | 170091480 | |||||
| chr3:170091502
|
T | C | 1 | a0001c0001t0042 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5728A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 5728 | chr3 | 170091502 | |||||
| chr3:170091521
|
T | C | 1 | a0001c0001t0008 | 8 | HG02055.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5709A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 5709 | chr3 | 170091521 | |||||
| chr3:170091561
|
C | G | 1 | a0001c0001t0048 | 1 | NA18998.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5669G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 5669 | chr3 | 170091561 | |||||
| chr3:170091771
|
A | C | 12 | a0001c0001t0002a0001c0001t0023a0001c0001t0026others(9): Show | 67 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*5459T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 5459 | chr3 | 170091771 | |||||
| chr3:170091772
|
C | A | 12 | a0001c0001t0002a0001c0001t0023a0001c0001t0026others(9): Show | 67 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*5458G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 5458 | chr3 | 170091772 | |||||
| chr3:170091786
|
AAGC | A | 19 | a0001c0001t0001a0001c0001t0009a0001c0001t0010others(16): Show | 107 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*5441_*5443delGCT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 5441 | chr3 | 170091786 | |||||
| chr3:170091814
|
G | A | 1 | a0001c0001t0050 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5416C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 5416 | chr3 | 170091814 | |||||
| chr3:170091949
|
T | C | 1 | a0001c0002t0024 | 2 | HG02071.hp2 HG03831.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5281A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 5281 | chr3 | 170091949 | |||||
| chr3:170092030
|
C | T | 1 | a0001c0001t0041 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5200G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 5200 | chr3 | 170092030 | |||||
| chr3:170092135
|
A | G | 41 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(38): Show | 205 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(202): Show |
3_prime_UTR_variant | MODIFIER | c.*5095T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 5095 | chr3 | 170092135 | |||||
| chr3:170092165
|
A | C | 3 | a0003c0005t0027a0003c0005t0028a0010c0007t0029 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5065T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 5065 | chr3 | 170092165 | |||||
| chr3:170092188
|
T | G | 1 | a0001c0001t0042 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5042A>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 5042 | chr3 | 170092188 | |||||
| chr3:170092303
|
A | G | 1 | a0001c0001t0008 | 8 | HG02055.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4927T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 4927 | chr3 | 170092303 | |||||
| chr3:170092329
|
TAAC | T | 1 | a0001c0001t0013 | 3 | HG01168.hp1 HG01192.hp2 HG01346.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4898_*4900delGTT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 4898 | chr3 | 170092329 | |||||
| chr3:170092366
|
T | C | 3 | a0003c0005t0027a0003c0005t0028a0010c0007t0029 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4864A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 4864 | chr3 | 170092366 | |||||
| chr3:170092555
|
G | A | 1 | a0001c0001t0051 | 1 | NA19085.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4675C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 4675 | chr3 | 170092555 | |||||
| chr3:170092753
|
T | G | 4 | a0001c0002t0005a0001c0002t0024a0001c0002t0044others(1): Show | 19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*4477A>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 4477 | chr3 | 170092753 | |||||
| chr3:170092766
|
C | T | 3 | a0003c0005t0027a0003c0005t0028a0010c0007t0029 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4464G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 4464 | chr3 | 170092766 | |||||
| chr3:170092896
|
A | G | 1 | a0001c0001t0054 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4334T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 4334 | chr3 | 170092896 | |||||
| chr3:170093139
|
G | A | 1 | a0001c0001t0043 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4091C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 4091 | chr3 | 170093139 | |||||
| chr3:170093236
|
C | T | 1 | a0001c0001t0035 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3994G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 3994 | chr3 | 170093236 | |||||
| chr3:170093251
|
G | C | 5 | a0001c0001t0004a0001c0001t0007a0001c0001t0055others(2): Show | 44 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*3979C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 3979 | chr3 | 170093251 | |||||
| chr3:170093412
|
A | G | 1 | a0001c0001t0033 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3818T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 3818 | chr3 | 170093412 | |||||
| chr3:170093590
|
T | C | 1 | a0001c0001t0052 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3640A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 3640 | chr3 | 170093590 | |||||
| chr3:170093612
|
T | C | 1 | a0001c0001t0053 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3618A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 3618 | chr3 | 170093612 | |||||
| chr3:170093978
|
A | G | 3 | a0003c0005t0027a0003c0005t0028a0010c0007t0029 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3252T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 3252 | chr3 | 170093978 | |||||
| chr3:170094269
|
A | G | 1 | a0001c0001t0034 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2961T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 2961 | chr3 | 170094269 | |||||
| chr3:170094327
|
A | G | 8 | a0001c0001t0004a0001c0001t0007a0001c0001t0008others(5): Show | 55 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*2903T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 2903 | chr3 | 170094327 | |||||
| chr3:170094363
|
C | T | 2 | a0003c0005t0027a0003c0005t0028 | 2 | HG01433.hp1 HG02055.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2867G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 2867 | chr3 | 170094363 | |||||
| chr3:170094530
|
C | G | 3 | a0001c0001t0012a0001c0001t0045a0001c0001t0054 | 6 | HG01167.hp1 HG01169.hp1 HG02818.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2700G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 2700 | chr3 | 170094530 | |||||
| chr3:170095162
|
T | C | 4 | a0001c0002t0005a0001c0002t0024a0001c0002t0044others(1): Show | 19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2068A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 2068 | chr3 | 170095162 | |||||
| chr3:170095234
|
T | C | 1 | a0001c0001t0056 | 1 | NA19003.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1996A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 1996 | chr3 | 170095234 | |||||
| chr3:170095552
|
C | T | 38 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(35): Show | 185 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(182): Show |
3_prime_UTR_variant | MODIFIER | c.*1678G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 1678 | chr3 | 170095552 | |||||
| chr3:170095689
|
T | A | 2 | a0001c0001t0031a0001c0001t0032 | 2 | HG00639.hp1 HG02451.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1541A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 1541 | chr3 | 170095689 | |||||
| chr3:170095830
|
C | G | 1 | a0001c0001t0033 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1400G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 1400 | chr3 | 170095830 | |||||
| chr3:170095877
|
G | A | 2 | a0001c0001t0012a0001c0001t0054 | 5 | HG01167.hp1 HG01169.hp1 HG02922.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1353C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 1353 | chr3 | 170095877 | |||||
| chr3:170096188
|
AT | A | 7 | a0001c0001t0004a0001c0001t0007a0001c0001t0018others(4): Show | 47 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*1041delA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 1041 | chr3 | 170096188 | |||||
| chr3:170096330
|
C | T | 2 | a0001c0001t0031a0001c0001t0032 | 2 | HG00639.hp1 HG02451.hp2 |
3_prime_UTR_variant | MODIFIER | c.*900G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 900 | chr3 | 170096330 | |||||
| chr3:170096338
|
C | T | 1 | a0001c0001t0030 | 1 | NA18955.hp1 | 3_prime_UTR_variant | MODIFIER | c.*892G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 892 | chr3 | 170096338 | |||||
| chr3:170096454
|
A | C | 3 | a0003c0005t0027a0003c0005t0028a0010c0007t0029 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*776T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 776 | chr3 | 170096454 | |||||
| chr3:170096943
|
T | C | 2 | a0001c0001t0019a0001c0001t0057 | 4 | HG01243.hp1 HG02572.hp2 HG02922.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*287A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 15/15 | 287 | chr3 | 170096943 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:170097444
|
C | T | 7 | a0001c0001t0006g0004a0001c0001t0006g0141a0001c0001t0006g0189others(4): Show | 7 | HG01884.hp1 HG02109.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2834-60G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170097444 | ||||||
| chr3:170097621
|
T | C | 19 | a0001c0002t0005g0305a0001c0002t0005g0306a0001c0002t0005g0307others(16): Show | 19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.2834-237A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170097621 | ||||||
| chr3:170097898
|
A | C | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2834-514T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170097898 | ||||||
| chr3:170098075
|
C | T | 1 | a0001c0001t0042g0194 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2834-691G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170098075 | ||||||
| chr3:170098216
|
A | T | 1 | a0002c0004t0017g0196 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2834-832T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170098216 | ||||||
| chr3:170098551
|
A | G | 1 | a0001c0001t0052g0243 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2834-1167T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170098551 | ||||||
| chr3:170098559
|
A | T | 1 | a0001c0013t0002g0213 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2834-1175T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170098559 | ||||||
| chr3:170098560
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2834-1176C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170098560 | ||||||
| chr3:170098721
|
A | G | 1 | a0001c0001t0004g0151 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2834-1337T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170098721 | ||||||
| chr3:170098722
|
C | T | 192 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(189): Show | 194 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.2834-1338G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170098722 | ||||||
| chr3:170099141
|
T | A | 1 | a0001c0001t0043g0030 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2834-1757A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170099141 | ||||||
| chr3:170099500
|
G | A | 3 | a0001c0001t0010g0028a0001c0001t0010g0029a0001c0001t0043g0030 | 3 | HG02615.hp1 HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2834-2116C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170099500 | ||||||
| chr3:170099575
|
G | A | 1 | a0001c0001t0004g0157 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2834-2191C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170099575 | ||||||
| chr3:170099667
|
T | C | 3 | a0001c0001t0010g0028a0001c0001t0010g0029a0001c0001t0043g0030 | 3 | HG02615.hp1 HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2834-2283A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170099667 | ||||||
| chr3:170099834
|
A | C | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2834-2450T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170099834 | ||||||
| chr3:170099898
|
C | T | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2834-2514G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170099898 | ||||||
| chr3:170099973
|
T | C | 2 | a0003c0005t0027g0324a0003c0005t0028g0325 | 2 | HG01433.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.2833+2506A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170099973 | ||||||
| chr3:170100078
|
A | G | 2 | a0001c0001t0001g0094a0001c0001t0035g0304 | 2 | HG00323.hp1 HG00642.hp1 |
intron_variant | MODIFIER | c.2833+2401T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170100078 | ||||||
| chr3:170100079
|
C | T | 115 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(112): Show | 116 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.2833+2400G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170100079 | ||||||
| chr3:170100267
|
T | G | 3 | a0001c0001t0010g0028a0001c0001t0010g0029a0001c0001t0043g0030 | 3 | HG02615.hp1 HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2833+2212A>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170100267 | ||||||
| chr3:170100377
|
G | C | 1 | a0001c0001t0008g0177 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2833+2102C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170100377 | ||||||
| chr3:170100589
|
T | C | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2833+1890A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170100589 | ||||||
| chr3:170100733
|
T | C | 19 | a0001c0002t0005g0305a0001c0002t0005g0306a0001c0002t0005g0307others(16): Show | 19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.2833+1746A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170100733 | ||||||
| chr3:170100849
|
T | C | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2833+1630A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170100849 | ||||||
| chr3:170100868
|
T | C | 1 | a0001c0001t0003g0202 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2833+1611A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170100868 | ||||||
| chr3:170100881
|
G | A | 67 | a0001c0001t0002g0118a0001c0001t0002g0121a0001c0001t0002g0123others(64): Show | 67 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.2833+1598C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170100881 | ||||||
| chr3:170101205
|
G | C | 1 | a0001c0001t0025g0253 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2833+1274C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170101205 | ||||||
| chr3:170101229
|
C | A | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2833+1250G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170101229 | ||||||
| chr3:170101557
|
G | A | 2 | a0001c0001t0031g0114a0001c0001t0032g0115 | 2 | HG00639.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.2833+922C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170101557 | ||||||
| chr3:170101705
|
C | G | 1 | a0001c0001t0042g0194 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2833+774G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170101705 | ||||||
| chr3:170101896
|
GCTCT | G | 4 | a0001c0001t0006g0141a0003c0005t0027g0324a0003c0005t0028g0325others(1): Show | 4 | HG01433.hp1 HG02055.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2833+579_2833+582d others(6): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170101896 | ||||||
| chr3:170101988
|
C | A | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2833+491G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170101988 | ||||||
| chr3:170102402
|
A | T | 3 | a0001c0001t0001g0073a0001c0001t0001g0084a0001c0001t0010g0014 | 3 | HG01123.hp2 HG01192.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2833+77T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170102402 | ||||||
| chr3:170102403
|
A | G | 1 | a0001c0001t0007g0149 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2833+76T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 14/14 | chr3 | 170102403 | ||||||
| chr3:170102798
|
A | G | 1 | a0001c0001t0003g0260 | 1 | NA19240.hp2 | splice_region_variant&intron_variant | LOW | c.2601+4T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 13/14 | chr3 | 170102798 | ||||||
| chr3:170103016
|
C | T | 1 | a0001c0001t0018g0140 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2469-82G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170103016 | ||||||
| chr3:170103019
|
TG | T | 4 | a0001c0001t0019g0001a0003c0005t0027g0324a0003c0005t0028g0325others(1): Show | 6 | HG01243.hp1 HG01433.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.2469-86delC | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170103019 | ||||||
| chr3:170103081
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2469-147C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170103081 | ||||||
| chr3:170103173
|
G | C | 2 | a0001c0001t0009g0002a0001c0001t0009g0064 | 3 | HG01257.hp2 HG01258.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.2469-239C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170103173 | ||||||
| chr3:170103238
|
C | T | 5 | a0001c0001t0019g0001a0001c0001t0037g0099a0003c0005t0027g0324others(2): Show | 7 | HG01243.hp1 HG01433.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2469-304G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170103238 | ||||||
| chr3:170103477
|
T | C | 1 | a0001c0001t0004g0159 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2469-543A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170103477 | ||||||
| chr3:170103513
|
CTCTT | C | 4 | a0001c0001t0019g0001a0003c0005t0027g0324a0003c0005t0028g0325others(1): Show | 6 | HG01243.hp1 HG01433.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.2469-583_2469-580d others(6): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170103513 | ||||||
| chr3:170103577
|
A | G | 8 | a0001c0001t0008g0113a0001c0001t0008g0116a0001c0001t0008g0117others(5): Show | 8 | HG02055.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.2469-643T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170103577 | ||||||
| chr3:170103887
|
C | T | 5 | a0001c0001t0016g0206a0001c0001t0016g0282a0002c0004t0017g0062others(2): Show | 5 | HG01884.hp2 HG02109.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.2469-953G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170103887 | ||||||
| chr3:170103898
|
C | T | 5 | a0001c0001t0001g0011a0001c0001t0001g0036a0001c0001t0001g0037others(2): Show | 5 | HG01256.hp2 HG01515.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.2469-964G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170103898 | ||||||
| chr3:170103899
|
G | A | 1 | a0001c0001t0007g0149 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2469-965C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170103899 | ||||||
| chr3:170104413
|
T | C | 54 | a0001c0001t0004g0005a0001c0001t0004g0006a0001c0001t0004g0127others(51): Show | 55 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.2469-1479A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170104413 | ||||||
| chr3:170104604
|
A | G | 19 | a0001c0002t0005g0305a0001c0002t0005g0306a0001c0002t0005g0307others(16): Show | 19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.2469-1670T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170104604 | ||||||
| chr3:170104790
|
C | G | 1 | a0001c0001t0003g0202 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2469-1856G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170104790 | ||||||
| chr3:170104802
|
G | A | 4 | a0001c0001t0019g0001a0003c0005t0027g0324a0003c0005t0028g0325others(1): Show | 6 | HG01243.hp1 HG01433.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.2469-1868C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170104802 | ||||||
| chr3:170104838
|
G | A | 2 | a0001c0003t0006g0293a0001c0003t0006g0296 | 2 | NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2469-1904C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170104838 | ||||||
| chr3:170104966
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2468+1866C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170104966 | ||||||
| chr3:170105234
|
T | C | 3 | a0001c0001t0010g0028a0001c0001t0010g0029a0001c0001t0043g0030 | 3 | HG02615.hp1 HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2468+1598A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170105234 | ||||||
| chr3:170105308
|
T | C | 46 | a0001c0001t0004g0005a0001c0001t0004g0006a0001c0001t0004g0127others(43): Show | 47 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.2468+1524A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170105308 | ||||||
| chr3:170105595
|
C | T | 1 | a0001c0001t0003g0208 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2468+1237G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170105595 | ||||||
| chr3:170105699
|
G | C | 4 | a0001c0001t0003g0179a0001c0001t0003g0209a0001c0001t0003g0210others(1): Show | 4 | HG02145.hp1 HG02970.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2468+1133C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170105699 | ||||||
| chr3:170105888
|
T | A | 2 | a0001c0001t0004g0165a0001c0001t0004g0174 | 2 | HG02486.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2468+944A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170105888 | ||||||
| chr3:170105965
|
A | G | 2 | a0001c0001t0021g0085a0001c0001t0021g0088 | 2 | HG03239.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.2468+867T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170105965 | ||||||
| chr3:170106038
|
C | T | 6 | a0001c0001t0016g0205a0001c0001t0016g0206a0001c0001t0016g0282others(3): Show | 6 | HG01884.hp2 HG02109.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2468+794G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170106038 | ||||||
| chr3:170106139
|
G | C | 1 | a0001c0001t0001g0093 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2468+693C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170106139 | ||||||
| chr3:170106160
|
C | A | 4 | a0001c0001t0002g0270a0001c0001t0002g0271a0001c0001t0002g0272others(1): Show | 4 | NA18747.hp1 NA18942.hp1 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.2468+672G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170106160 | ||||||
| chr3:170106170
|
C | G | 17 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(14): Show | 17 | HG00544.hp2 HG00558.hp2 HG00621.hp2 others(14): Show |
intron_variant | MODIFIER | c.2468+662G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170106170 | ||||||
| chr3:170106199
|
AAG | A | 19 | a0001c0002t0005g0305a0001c0002t0005g0306a0001c0002t0005g0307others(16): Show | 19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.2468+631_2468+632d others(4): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170106199 | ||||||
| chr3:170106293
|
A | C | 1 | a0001c0001t0041g0207 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2468+539T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170106293 | ||||||
| chr3:170106397
|
T | C | 1 | a0001c0001t0015g0255 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2468+435A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170106397 | ||||||
| chr3:170106545
|
C | A | 1 | a0001c0001t0003g0233 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2468+287G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170106545 | ||||||
| chr3:170106639
|
G | A | 321 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(318): Show | 325 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.2468+193C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 12/14 | chr3 | 170106639 | ||||||
| chr3:170107219
|
T | TA | 116 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(113): Show | 117 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.2354-274dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170107219 | ||||||
| chr3:170107309
|
G | C | 1 | a0001c0001t0003g0208 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2354-363C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170107309 | ||||||
| chr3:170107417
|
T | C | 200 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(197): Show | 204 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.2354-471A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170107417 | ||||||
| chr3:170107678
|
G | A | 1 | a0001c0001t0007g0142 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2354-732C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170107678 | ||||||
| chr3:170107688
|
T | TCA | 120 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(117): Show | 123 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.2354-744_2354-743d others(4): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170107688 | ||||||
| chr3:170107857
|
C | T | 4 | a0001c0003t0006g0293a0001c0003t0006g0294a0001c0003t0006g0295others(1): Show | 4 | HG02976.hp2 HG03453.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.2354-911G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170107857 | ||||||
| chr3:170107858
|
G | A | 1 | a0001c0001t0033g0239 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2354-912C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170107858 | ||||||
| chr3:170107899
|
C | A | 1 | a0001c0001t0001g0108 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2354-953G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170107899 | ||||||
| chr3:170108083
|
T | C | 70 | a0001c0001t0002g0118a0001c0001t0002g0121a0001c0001t0002g0123others(67): Show | 70 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.2354-1137A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170108083 | ||||||
| chr3:170108122
|
T | C | 1 | a0001c0001t0042g0194 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2354-1176A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170108122 | ||||||
| chr3:170108264
|
G | A | 1 | a0001c0001t0003g0197 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2354-1318C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170108264 | ||||||
| chr3:170108312
|
T | C | 3 | a0001c0001t0001g0037a0001c0001t0001g0303a0007c0009t0001g0019 | 3 | HG01256.hp2 HG01978.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.2354-1366A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170108312 | ||||||
| chr3:170108351
|
A | C | 3 | a0001c0001t0010g0028a0001c0001t0010g0029a0001c0001t0043g0030 | 3 | HG02615.hp1 HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2354-1405T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170108351 | ||||||
| chr3:170108357
|
T | C | 7 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0044others(4): Show | 7 | HG01433.hp2 HG02300.hp1 NA18957.hp1 others(4): Show |
intron_variant | MODIFIER | c.2354-1411A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170108357 | ||||||
| chr3:170108518
|
A | G | 3 | a0001c0001t0010g0028a0001c0001t0010g0029a0001c0001t0043g0030 | 3 | HG02615.hp1 HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2354-1572T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170108518 | ||||||
| chr3:170108565
|
A | G | 2 | a0001c0002t0005g0306a0001c0002t0005g0319 | 2 | NA18964.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.2354-1619T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170108565 | ||||||
| chr3:170108660
|
A | G | 1 | a0001c0001t0026g0274 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2354-1714T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170108660 | ||||||
| chr3:170108871
|
C | G | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2354-1925G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170108871 | ||||||
| chr3:170108984
|
GAGT | G | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2354-2041_2354-203 others(7): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170108984 | ||||||
| chr3:170109317
|
C | T | 2 | a0001c0001t0001g0106a0001c0001t0001g0290 | 2 | HG02056.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.2354-2371G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170109317 | ||||||
| chr3:170109365
|
G | A | 116 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(113): Show | 117 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.2354-2419C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170109365 | ||||||
| chr3:170109404
|
A | G | 3 | a0001c0001t0014g0109a0001c0001t0014g0110a0001c0001t0014g0111 | 3 | HG02257.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2354-2458T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170109404 | ||||||
| chr3:170109884
|
C | G | 8 | a0001c0001t0008g0113a0001c0001t0008g0116a0001c0001t0008g0117others(5): Show | 8 | HG02055.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.2354-2938G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170109884 | ||||||
| chr3:170109966
|
TA | T | 192 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(189): Show | 194 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.2354-3021delT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170109966 | ||||||
| chr3:170110165
|
T | C | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2353+3195A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170110165 | ||||||
| chr3:170110221
|
G | A | 7 | a0001c0001t0015g0254a0001c0001t0015g0255a0001c0001t0015g0256others(4): Show | 9 | HG01243.hp1 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.2353+3139C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170110221 | ||||||
| chr3:170110299
|
T | C | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2353+3061A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170110299 | ||||||
| chr3:170110327
|
G | A | 6 | a0001c0001t0012g0100a0001c0001t0012g0102a0001c0001t0012g0103others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2353+3033C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170110327 | ||||||
| chr3:170110346
|
AC | A | 6 | a0001c0001t0012g0100a0001c0001t0012g0102a0001c0001t0012g0103others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2353+3013delG | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170110346 | ||||||
| chr3:170110499
|
T | C | 5 | a0001c0001t0015g0254a0001c0001t0015g0255a0001c0001t0015g0256others(2): Show | 7 | HG01243.hp1 HG02258.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.2353+2861A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170110499 | ||||||
| chr3:170110500
|
C | T | 2 | a0001c0001t0002g0214a0001c0001t0002g0286 | 2 | HG00609.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.2353+2860G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170110500 | ||||||
| chr3:170110583
|
C | A | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2353+2777G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170110583 | ||||||
| chr3:170110595
|
T | A | 1 | a0001c0001t0031g0114 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2353+2765A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170110595 | ||||||
| chr3:170110855
|
C | T | 2 | a0001c0001t0031g0114a0001c0001t0032g0115 | 2 | HG00639.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.2353+2505G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170110855 | ||||||
| chr3:170111261
|
A | AAAAG | 16 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0017others(13): Show | 16 | HG00323.hp2 HG00558.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.2353+2098_2353+209 others(8): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111261 | ||||||
| chr3:170111261
|
A | AGAAG | 10 | a0001c0001t0002g0235a0001c0001t0002g0241a0001c0001t0002g0242others(7): Show | 10 | HG00423.hp2 HG02280.hp2 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.2353+2095_2353+209 others(8): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111261 | ||||||
| chr3:170111261
|
A | AGAAGGAA others(5): Show |
1 | a0001c0001t0002g0133 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2353+2087_2353+209 others(16): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111261 | ||||||
| chr3:170111261
|
AGAAG | A | 78 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0026others(75): Show | 79 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.2353+2095_2353+209 others(8): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111261 | ||||||
| chr3:170111261
|
AGAAGGAA others(1): Show |
A | 36 | a0001c0001t0001g0108a0001c0001t0002g0129a0001c0001t0002g0130others(33): Show | 38 | HG00140.hp2 HG00621.hp1 HG01123.hp1 others(35): Show |
intron_variant | MODIFIER | c.2353+2091_2353+209 others(12): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111261 | ||||||
| chr3:170111261
|
AGAAGGAA others(5): Show |
A | 33 | a0001c0001t0001g0031a0001c0001t0001g0079a0001c0001t0002g0181others(30): Show | 33 | HG00609.hp1 HG00639.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.2353+2087_2353+209 others(16): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111261 | ||||||
| chr3:170111261
|
AGAAGGAA others(9): Show |
A | 18 | a0001c0001t0002g0214a0001c0001t0002g0236a0001c0001t0003g0208others(15): Show | 18 | HG00423.hp1 HG00558.hp1 HG00673.hp2 others(15): Show |
intron_variant | MODIFIER | c.2353+2083_2353+209 others(20): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111261 | ||||||
| chr3:170111261
|
AGAAGGAA others(13): Show |
A | 11 | a0001c0001t0008g0113a0001c0001t0008g0116a0001c0001t0008g0117others(8): Show | 11 | HG02027.hp2 HG02055.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.2353+2079_2353+209 others(24): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111261 | ||||||
| chr3:170111261
|
AGAAGGAA others(17): Show |
A | 1 | a0001c0001t0008g0175 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2353+2075_2353+209 others(28): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111261 | ||||||
| chr3:170111262
|
G | A | 37 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(34): Show | 38 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.2353+2098C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111262 | ||||||
| chr3:170111266
|
G | A | 4 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0074others(1): Show | 4 | HG02293.hp2 NA18973.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.2353+2094C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111266 | ||||||
| chr3:170111274
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2353+2086C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111274 | ||||||
| chr3:170111297
|
GGAAGGAA others(21): Show |
G | 1 | a0010c0007t0029g0323 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2353+2035_2353+206 others(32): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111297 | ||||||
| chr3:170111301
|
GGAAGGAA others(17): Show |
G | 2 | a0003c0005t0027g0324a0003c0005t0028g0325 | 2 | HG01433.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.2353+2035_2353+205 others(28): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111301 | ||||||
| chr3:170111305
|
G | C | 20 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0017others(17): Show | 20 | HG00323.hp2 HG00558.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.2353+2055C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111305 | ||||||
| chr3:170111309
|
G | C | 67 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(64): Show | 67 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.2353+2051C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111309 | ||||||
| chr3:170111309
|
G | GGAACGAA others(1): Show |
18 | a0001c0001t0001g0013a0001c0001t0001g0018a0001c0001t0001g0027others(15): Show | 18 | HG00280.hp1 HG00438.hp1 HG00597.hp2 others(15): Show |
intron_variant | MODIFIER | c.2353+2050_2353+205 others(12): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111309 | ||||||
| chr3:170111309
|
G | GGAACGAA others(5): Show |
1 | a0001c0001t0011g0087 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2353+2050_2353+205 others(16): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111309 | ||||||
| chr3:170111309
|
GGAAGGAA others(5): Show |
G | 1 | a0001c0001t0047g0212 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2353+2039_2353+205 others(16): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111309 | ||||||
| chr3:170111313
|
G | C | 101 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(98): Show | 101 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.2353+2047C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111313 | ||||||
| chr3:170111313
|
G | GGAACGAA others(1): Show |
4 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0106others(1): Show | 4 | HG01255.hp1 HG02056.hp2 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.2353+2046_2353+204 others(12): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111313 | ||||||
| chr3:170111313
|
G | GGAACGAA others(5): Show |
6 | a0001c0001t0001g0015a0001c0001t0009g0002a0001c0001t0009g0064others(3): Show | 7 | HG01109.hp1 HG01257.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.2353+2046_2353+204 others(16): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111313 | ||||||
| chr3:170111313
|
GGAAGGAA others(1): Show |
G | 9 | a0001c0001t0003g0228a0001c0001t0003g0232a0001c0001t0003g0267others(6): Show | 9 | HG00735.hp2 HG01106.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.2353+2039_2353+204 others(12): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111313 | ||||||
| chr3:170111317
|
G | C | 127 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(124): Show | 128 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.2353+2043C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111317 | ||||||
| chr3:170111317
|
G | GGAACGAA others(9): Show |
1 | a0001c0001t0001g0080 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2353+2042_2353+204 others(20): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111317 | ||||||
| chr3:170111317
|
GGAAC | G | 8 | a0001c0001t0003g0231a0001c0001t0003g0233a0001c0001t0003g0261others(5): Show | 8 | HG01081.hp1 HG01109.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.2353+2039_2353+204 others(8): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111317 | ||||||
| chr3:170111321
|
C | G | 3 | a0001c0001t0003g0179a0001c0001t0003g0211a0001c0001t0003g0227 | 3 | HG00140.hp1 HG02145.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2353+2039G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111321 | ||||||
| chr3:170111325
|
C | A | 2 | a0001c0001t0003g0262a0001c0001t0003g0265 | 2 | HG01175.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.2353+2035G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111325 | ||||||
| chr3:170111330
|
G | A | 2 | a0001c0001t0003g0262a0001c0001t0003g0265 | 2 | HG01175.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.2353+2030C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111330 | ||||||
| chr3:170111341
|
A | G | 2 | a0001c0001t0003g0262a0001c0001t0003g0265 | 2 | HG01175.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.2353+2019T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111341 | ||||||
| chr3:170111345
|
C | A | 2 | a0001c0001t0003g0262a0001c0001t0003g0265 | 2 | HG01175.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.2353+2015G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111345 | ||||||
| chr3:170111345
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2353+2015G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111345 | ||||||
| chr3:170111348
|
A | G | 2 | a0001c0001t0003g0262a0001c0001t0003g0265 | 2 | HG01175.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.2353+2012T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111348 | ||||||
| chr3:170111352
|
G | GAAAGGGA others(8): Show |
1 | a0001c0001t0003g0263 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2353+1993_2353+200 others(19): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111352 | ||||||
| chr3:170111378
|
A | G | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2353+1982T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111378 | ||||||
| chr3:170111384
|
G | A | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2353+1976C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111384 | ||||||
| chr3:170111392
|
A | G | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2353+1968T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111392 | ||||||
| chr3:170111393
|
A | G | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2353+1967T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111393 | ||||||
| chr3:170111394
|
G | A | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2353+1966C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111394 | ||||||
| chr3:170111394
|
G | GAGGAAGG others(9): Show |
1 | a0001c0002t0005g0311 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2353+1950_2353+196 others(20): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111394 | ||||||
| chr3:170111394
|
G | GAGGAAGG others(17): Show |
2 | a0001c0002t0044g0316a0008c0014t0005g0321 | 2 | HG02027.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.2353+1942_2353+196 others(28): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111394 | ||||||
| chr3:170111394
|
G | GAGGAAGG others(21): Show |
10 | a0001c0002t0005g0305a0001c0002t0005g0307a0001c0002t0005g0308others(7): Show | 10 | HG00423.hp1 HG00558.hp1 HG00673.hp2 others(7): Show |
intron_variant | MODIFIER | c.2353+1965_2353+196 others(32): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111394 | ||||||
| chr3:170111394
|
G | GAGGAAGG others(25): Show |
5 | a0001c0002t0005g0310a0001c0002t0005g0318a0001c0002t0005g0319others(2): Show | 5 | HG02015.hp1 NA18951.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.2353+1965_2353+196 others(36): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111394 | ||||||
| chr3:170111394
|
G | GAGGAAGG others(29): Show |
1 | a0001c0002t0005g0306 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2353+1965_2353+196 others(40): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111394 | ||||||
| chr3:170111723
|
TAAAACGG others(15): Show |
T | 8 | a0001c0001t0008g0113a0001c0001t0008g0116a0001c0001t0008g0117others(5): Show | 8 | HG02055.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.2353+1615_2353+163 others(26): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111723 | ||||||
| chr3:170111756
|
A | C | 1 | a0001c0001t0037g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2353+1604T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111756 | ||||||
| chr3:170111796
|
G | C | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2353+1564C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170111796 | ||||||
| chr3:170112021
|
T | C | 1 | a0001c0001t0008g0175 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2353+1339A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170112021 | ||||||
| chr3:170112067
|
C | T | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2353+1293G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170112067 | ||||||
| chr3:170112080
|
T | C | 115 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(112): Show | 116 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.2353+1280A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170112080 | ||||||
| chr3:170112144
|
C | T | 8 | a0001c0001t0008g0113a0001c0001t0008g0116a0001c0001t0008g0117others(5): Show | 8 | HG02055.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.2353+1216G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170112144 | ||||||
| chr3:170112190
|
A | G | 1 | a0001c0001t0018g0140 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2353+1170T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170112190 | ||||||
| chr3:170112379
|
TTA | T | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2353+979_2353+980d others(4): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170112379 | ||||||
| chr3:170112386
|
T | C | 54 | a0001c0001t0004g0005a0001c0001t0004g0006a0001c0001t0004g0127others(51): Show | 55 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.2353+974A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170112386 | ||||||
| chr3:170112392
|
TA | T | 5 | a0001c0001t0011g0087a0001c0001t0014g0109a0001c0001t0014g0110others(2): Show | 5 | HG02132.hp2 HG02257.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2353+967delT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170112392 | ||||||
| chr3:170112394
|
TA | T | 155 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(152): Show | 157 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.2353+965delT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170112394 | ||||||
| chr3:170112395
|
A | T | 12 | a0001c0001t0002g0130a0001c0001t0002g0184a0001c0001t0002g0185others(9): Show | 12 | HG00609.hp1 HG02080.hp2 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.2353+965T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170112395 | ||||||
| chr3:170112395
|
AT | A | 22 | a0001c0001t0001g0033a0001c0001t0001g0044a0001c0001t0032g0115others(19): Show | 22 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.2353+964delA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170112395 | ||||||
| chr3:170112439
|
G | T | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2353+921C>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170112439 | ||||||
| chr3:170112486
|
G | C | 1 | a0001c0001t0003g0260 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2353+874C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170112486 | ||||||
| chr3:170112505
|
A | G | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2353+855T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170112505 | ||||||
| chr3:170112513
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2353+847C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170112513 | ||||||
| chr3:170112524
|
A | AT | 112 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(109): Show | 113 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.2353+835dupA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170112524 | ||||||
| chr3:170112524
|
AT | A | 7 | a0001c0001t0002g0276a0001c0001t0004g0128a0001c0001t0004g0148others(4): Show | 7 | HG01168.hp1 HG01433.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2353+835delA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170112524 | ||||||
| chr3:170112610
|
G | A | 1 | a0001c0001t0034g0089 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2353+750C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170112610 | ||||||
| chr3:170112671
|
A | G | 54 | a0001c0001t0004g0005a0001c0001t0004g0006a0001c0001t0004g0127others(51): Show | 55 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.2353+689T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170112671 | ||||||
| chr3:170112807
|
A | G | 1 | a0001c0001t0031g0114 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2353+553T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170112807 | ||||||
| chr3:170113153
|
G | A | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2353+207C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 11/14 | chr3 | 170113153 | ||||||
| chr3:170113714
|
C | T | 3 | a0001c0001t0001g0037a0001c0001t0001g0303a0007c0009t0001g0019 | 3 | HG01256.hp2 HG01978.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.2194-195G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170113714 | ||||||
| chr3:170113895
|
A | C | 1 | a0001c0001t0002g0124 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2194-376T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170113895 | ||||||
| chr3:170114164
|
C | T | 1 | a0001c0001t0042g0194 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2194-645G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170114164 | ||||||
| chr3:170114165
|
G | A | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2194-646C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170114165 | ||||||
| chr3:170114304
|
C | T | 1 | a0001c0001t0042g0194 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2194-785G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170114304 | ||||||
| chr3:170114314
|
T | C | 4 | a0001c0001t0002g0270a0001c0001t0002g0271a0001c0001t0002g0272others(1): Show | 4 | NA18747.hp1 NA18942.hp1 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.2194-795A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170114314 | ||||||
| chr3:170114328
|
C | T | 119 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(116): Show | 120 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.2194-809G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170114328 | ||||||
| chr3:170114558
|
C | T | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2194-1039G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170114558 | ||||||
| chr3:170114727
|
G | A | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2194-1208C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170114727 | ||||||
| chr3:170114758
|
C | G | 1 | a0001c0001t0054g0105 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2194-1239G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170114758 | ||||||
| chr3:170114766
|
T | A | 1 | a0001c0001t0001g0037 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2194-1247A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170114766 | ||||||
| chr3:170114971
|
A | G | 1 | a0001c0001t0045g0101 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2194-1452T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170114971 | ||||||
| chr3:170115152
|
T | C | 1 | a0001c0001t0008g0177 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2194-1633A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170115152 | ||||||
| chr3:170115319
|
AAGG | A | 47 | a0001c0001t0004g0005a0001c0001t0004g0006a0001c0001t0004g0127others(44): Show | 48 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.2194-1803_2194-180 others(7): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170115319 | ||||||
| chr3:170115350
|
ATATG | A | 5 | a0001c0001t0002g0278a0001c0001t0003g0261a0001c0001t0008g0113others(2): Show | 5 | HG02486.hp1 HG02622.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2194-1835_2194-183 others(8): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170115350 | ||||||
| chr3:170115405
|
A | T | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2193+1821T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170115405 | ||||||
| chr3:170115459
|
A | G | 46 | a0001c0001t0004g0005a0001c0001t0004g0006a0001c0001t0004g0127others(43): Show | 47 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.2193+1767T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170115459 | ||||||
| chr3:170115540
|
T | C | 3 | a0001c0001t0014g0109a0001c0001t0014g0110a0001c0001t0014g0111 | 3 | HG02257.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2193+1686A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170115540 | ||||||
| chr3:170115877
|
T | TCA | 17 | a0001c0001t0002g0215a0001c0001t0002g0244a0001c0001t0002g0246others(14): Show | 19 | HG01243.hp1 HG01884.hp1 HG02572.hp2 others(16): Show |
intron_variant | MODIFIER | c.2193+1347_2193+134 others(6): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170115877 | ||||||
| chr3:170115877
|
T | TCACA | 9 | a0001c0001t0001g0086a0001c0001t0006g0004a0001c0001t0006g0141others(6): Show | 9 | HG00741.hp1 HG02109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.2193+1345_2193+134 others(8): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170115877 | ||||||
| chr3:170115877
|
T | TCACACAC others(1): Show |
127 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0031others(124): Show | 129 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.2193+1341_2193+134 others(12): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170115877 | ||||||
| chr3:170115877
|
T | TCACACAC others(3): Show |
34 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(31): Show | 34 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.2193+1339_2193+134 others(14): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170115877 | ||||||
| chr3:170115877
|
T | TCACACAC others(5): Show |
4 | a0001c0001t0001g0055a0001c0001t0001g0112a0001c0001t0012g0104others(1): Show | 4 | HG01361.hp2 HG03098.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.2193+1337_2193+134 others(16): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170115877 | ||||||
| chr3:170115877
|
T | TCACACAC others(9): Show |
3 | a0001c0001t0010g0028a0001c0001t0010g0029a0001c0001t0043g0030 | 3 | HG02615.hp1 HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2193+1333_2193+134 others(20): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170115877 | ||||||
| chr3:170115877
|
T | TCACACAC others(13): Show |
3 | a0001c0002t0005g0307a0001c0002t0005g0308a0001c0002t0005g0314 | 3 | HG00558.hp1 NA18975.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.2193+1329_2193+134 others(24): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170115877 | ||||||
| chr3:170115877
|
T | TCACACAC others(17): Show |
1 | a0001c0002t0005g0326 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2193+1325_2193+134 others(28): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170115877 | ||||||
| chr3:170115877
|
T | TCTCACAC others(5): Show |
1 | a0001c0001t0010g0020 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2193+1348_2193+134 others(16): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170115877 | ||||||
| chr3:170115877
|
TCA | T | 16 | a0001c0002t0005g0305a0001c0002t0005g0306a0001c0002t0005g0310others(13): Show | 16 | HG00408.hp1 HG00423.hp1 HG00673.hp2 others(13): Show |
intron_variant | MODIFIER | c.2193+1347_2193+134 others(6): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170115877 | ||||||
| chr3:170115909
|
T | C | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2193+1317A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170115909 | ||||||
| chr3:170116006
|
A | C | 3 | a0001c0001t0010g0028a0001c0001t0010g0029a0001c0001t0043g0030 | 3 | HG02615.hp1 HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2193+1220T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170116006 | ||||||
| chr3:170116069
|
T | C | 7 | a0001c0001t0006g0004a0001c0001t0006g0141a0001c0001t0006g0189others(4): Show | 7 | HG01884.hp1 HG02109.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2193+1157A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170116069 | ||||||
| chr3:170116111
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2193+1115C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170116111 | ||||||
| chr3:170116132
|
G | C | 199 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(196): Show | 201 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.2193+1094C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170116132 | ||||||
| chr3:170116319
|
C | A | 1 | a0001c0003t0006g0296 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2193+907G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170116319 | ||||||
| chr3:170116320
|
T | C | 25 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0035others(22): Show | 25 | HG00673.hp1 HG01261.hp2 HG01361.hp2 others(22): Show |
intron_variant | MODIFIER | c.2193+906A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170116320 | ||||||
| chr3:170116381
|
T | C | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2193+845A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170116381 | ||||||
| chr3:170116486
|
A | G | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2193+740T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170116486 | ||||||
| chr3:170116517
|
A | C | 1 | a0001c0001t0004g0166 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2193+709T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170116517 | ||||||
| chr3:170116570
|
A | C | 1 | a0001c0001t0001g0021 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2193+656T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170116570 | ||||||
| chr3:170116654
|
C | T | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2193+572G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170116654 | ||||||
| chr3:170116672
|
A | G | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2193+554T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170116672 | ||||||
| chr3:170116720
|
A | G | 325 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(322): Show | 329 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.2193+506T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170116720 | ||||||
| chr3:170116806
|
G | A | 1 | a0001c0001t0001g0056 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2193+420C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170116806 | ||||||
| chr3:170116865
|
C | T | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2193+361G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170116865 | ||||||
| chr3:170116909
|
TA | T | 315 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(312): Show | 319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.2193+316delT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170116909 | ||||||
| chr3:170117069
|
T | C | 1 | a0001c0001t0002g0217 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2193+157A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170117069 | ||||||
| chr3:170117164
|
G | A | 5 | a0001c0001t0015g0254a0001c0001t0015g0255a0001c0001t0015g0256others(2): Show | 7 | HG01243.hp1 HG02258.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.2193+62C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 10/14 | chr3 | 170117164 | ||||||
| chr3:170117479
|
G | GA | 24 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0083others(21): Show | 24 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(21): Show |
splice_region_variant&intron_variant | LOW | c.1943-4dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170117479 | ||||||
| chr3:170117480
|
A | G | 1 | a0001c0001t0003g0232 | 1 | HG02040.hp1 | splice_region_variant&intron_variant | LOW | c.1943-4T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170117480 | ||||||
| chr3:170117732
|
G | T | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1943-256C>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170117732 | ||||||
| chr3:170117785
|
G | GAGA | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1943-312_1943-310d others(5): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170117785 | ||||||
| chr3:170117832
|
T | TA | 21 | a0001c0001t0042g0194a0001c0002t0005g0305a0001c0002t0005g0306others(18): Show | 21 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(18): Show |
intron_variant | MODIFIER | c.1943-357dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170117832 | ||||||
| chr3:170117843
|
C | A | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1943-367G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170117843 | ||||||
| chr3:170117844
|
C | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0012 | 2 | NA19000.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1943-368G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170117844 | ||||||
| chr3:170117844
|
C | CA | 9 | a0001c0001t0001g0049a0001c0001t0002g0181a0001c0001t0003g0262others(6): Show | 9 | HG01175.hp1 HG01934.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.1943-369dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170117844 | ||||||
| chr3:170118337
|
C | T | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1943-861G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170118337 | ||||||
| chr3:170118344
|
C | G | 4 | a0001c0001t0003g0179a0001c0001t0003g0209a0001c0001t0003g0210others(1): Show | 4 | HG02145.hp1 HG02970.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1943-868G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170118344 | ||||||
| chr3:170118434
|
C | T | 3 | a0001c0001t0014g0109a0001c0001t0014g0110a0001c0001t0014g0111 | 3 | HG02257.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1943-958G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170118434 | ||||||
| chr3:170118562
|
C | A | 1 | a0001c0001t0011g0065 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1943-1086G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170118562 | ||||||
| chr3:170118575
|
A | C | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1943-1099T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170118575 | ||||||
| chr3:170119021
|
C | A | 2 | a0001c0003t0006g0293a0001c0003t0006g0296 | 2 | NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1943-1545G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170119021 | ||||||
| chr3:170119036
|
T | TA | 50 | a0001c0001t0002g0242a0001c0001t0003g0134a0001c0001t0004g0005others(47): Show | 51 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.1943-1561dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170119036 | ||||||
| chr3:170119036
|
T | TAAA | 18 | a0001c0002t0005g0305a0001c0002t0005g0306a0001c0002t0005g0307others(15): Show | 18 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(15): Show |
intron_variant | MODIFIER | c.1943-1563_1943-156 others(7): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170119036 | ||||||
| chr3:170119036
|
TA | T | 17 | a0001c0001t0002g0118a0001c0001t0002g0219a0001c0001t0002g0251others(14): Show | 17 | HG01167.hp1 HG01169.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.1943-1561delT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170119036 | ||||||
| chr3:170119432
|
T | C | 7 | a0001c0001t0006g0004a0001c0001t0006g0141a0001c0001t0006g0189others(4): Show | 7 | HG01884.hp1 HG02109.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1943-1956A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170119432 | ||||||
| chr3:170119627
|
C | T | 1 | a0001c0001t0004g0164 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1943-2151G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170119627 | ||||||
| chr3:170119711
|
C | T | 2 | a0001c0001t0021g0085a0001c0001t0021g0088 | 2 | HG03239.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1943-2235G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170119711 | ||||||
| chr3:170119731
|
C | T | 192 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(189): Show | 194 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1943-2255G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170119731 | ||||||
| chr3:170119745
|
T | C | 1 | a0001c0001t0004g0158 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1943-2269A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170119745 | ||||||
| chr3:170119756
|
A | G | 4 | a0001c0001t0002g0118a0001c0001t0002g0289a0001c0001t0049g0288others(1): Show | 4 | NA18959.hp2 NA18983.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1943-2280T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170119756 | ||||||
| chr3:170119830
|
T | TA | 56 | a0001c0001t0004g0005a0001c0001t0004g0006a0001c0001t0004g0127others(53): Show | 57 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.1943-2355dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170119830 | ||||||
| chr3:170119830
|
T | TAA | 7 | a0001c0001t0007g0126a0001c0001t0012g0100a0001c0001t0012g0102others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.1943-2356_1943-235 others(6): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170119830 | ||||||
| chr3:170119830
|
T | TAAA | 9 | a0001c0001t0010g0028a0001c0001t0010g0029a0001c0001t0014g0109others(6): Show | 9 | HG00639.hp1 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1943-2357_1943-235 others(7): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170119830 | ||||||
| chr3:170119830
|
TA | T | 6 | a0001c0001t0003g0179a0001c0001t0003g0211a0001c0001t0033g0239others(3): Show | 6 | HG02132.hp1 HG02145.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1943-2355delT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170119830 | ||||||
| chr3:170119844
|
A | AAAG | 18 | a0001c0002t0005g0305a0001c0002t0005g0306a0001c0002t0005g0307others(15): Show | 18 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(15): Show |
intron_variant | MODIFIER | c.1943-2369_1943-236 others(7): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170119844 | ||||||
| chr3:170119850
|
C | T | 1 | a0001c0001t0042g0194 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1943-2374G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170119850 | ||||||
| chr3:170119907
|
G | T | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1943-2431C>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170119907 | ||||||
| chr3:170119999
|
A | G | 46 | a0001c0001t0004g0005a0001c0001t0004g0006a0001c0001t0004g0127others(43): Show | 47 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.1943-2523T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170119999 | ||||||
| chr3:170120212
|
A | G | 155 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(152): Show | 157 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.1942+2379T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170120212 | ||||||
| chr3:170120415
|
G | A | 14 | a0001c0001t0010g0028a0001c0001t0010g0029a0001c0001t0012g0100others(11): Show | 14 | HG00639.hp1 HG01167.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.1942+2176C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170120415 | ||||||
| chr3:170120519
|
G | A | 5 | a0001c0001t0012g0100a0001c0001t0012g0102a0001c0001t0012g0103others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1942+2072C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170120519 | ||||||
| chr3:170120625
|
T | C | 2 | a0001c0001t0001g0108a0009c0010t0001g0107 | 2 | HG02257.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1942+1966A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170120625 | ||||||
| chr3:170120943
|
T | C | 1 | a0011c0006t0002g0122 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1942+1648A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170120943 | ||||||
| chr3:170120994
|
C | T | 1 | a0001c0001t0011g0087 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1942+1597G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170120994 | ||||||
| chr3:170121082
|
A | G | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1942+1509T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170121082 | ||||||
| chr3:170121317
|
A | G | 1 | a0001c0001t0003g0268 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1942+1274T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170121317 | ||||||
| chr3:170121318
|
G | C | 1 | a0010c0007t0029g0323 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1942+1273C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170121318 | ||||||
| chr3:170121430
|
C | T | 2 | a0003c0005t0027g0324a0003c0005t0028g0325 | 2 | HG01433.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.1942+1161G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170121430 | ||||||
| chr3:170121447
|
C | T | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1942+1144G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170121447 | ||||||
| chr3:170121451
|
G | C | 46 | a0001c0001t0004g0005a0001c0001t0004g0006a0001c0001t0004g0127others(43): Show | 47 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.1942+1140C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170121451 | ||||||
| chr3:170121540
|
T | C | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1942+1051A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170121540 | ||||||
| chr3:170121719
|
T | C | 19 | a0001c0002t0005g0305a0001c0002t0005g0306a0001c0002t0005g0307others(16): Show | 19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.1942+872A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170121719 | ||||||
| chr3:170121806
|
T | C | 1 | a0001c0001t0003g0233 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1942+785A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170121806 | ||||||
| chr3:170121910
|
T | C | 1 | a0001c0001t0002g0272 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1942+681A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170121910 | ||||||
| chr3:170121992
|
C | A | 1 | a0001c0001t0001g0034 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1942+599G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170121992 | ||||||
| chr3:170122049
|
T | C | 19 | a0001c0002t0005g0305a0001c0002t0005g0306a0001c0002t0005g0307others(16): Show | 19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.1942+542A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170122049 | ||||||
| chr3:170122303
|
T | C | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1942+288A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170122303 | ||||||
| chr3:170122540
|
ATTAACAT | A | 4 | a0001c0001t0003g0179a0001c0001t0003g0209a0001c0001t0003g0210others(1): Show | 4 | HG02145.hp1 HG02970.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1942+44_1942+50del others(7): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 9/14 | chr3 | 170122540 | ||||||
| chr3:170122778
|
T | G | 1 | a0001c0001t0025g0253 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1789-34A>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170122778 | ||||||
| chr3:170122826
|
C | A | 1 | a0001c0001t0001g0032 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1789-82G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170122826 | ||||||
| chr3:170122861
|
ACTACT | A | 4 | a0001c0001t0001g0073a0001c0001t0001g0084a0001c0001t0003g0231others(1): Show | 4 | HG01123.hp2 HG01192.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.1789-122_1789-118d others(7): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170122861 | ||||||
| chr3:170122866
|
TCTAA | T | 5 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0002g0247others(2): Show | 5 | NA18943.hp2 NA18944.hp2 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.1789-126_1789-123d others(6): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170122866 | ||||||
| chr3:170122874
|
A | G | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1789-130T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170122874 | ||||||
| chr3:170123139
|
G | A | 1 | a0001c0001t0002g0192 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1789-395C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170123139 | ||||||
| chr3:170123263
|
C | A | 1 | a0001c0003t0006g0296 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1789-519G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170123263 | ||||||
| chr3:170123356
|
T | TACACACA others(1): Show |
98 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(95): Show | 99 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.1789-620_1789-613d others(10): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170123356 | ||||||
| chr3:170123356
|
T | TACACACA others(3): Show |
2 | a0001c0001t0001g0082a0001c0001t0003g0231 | 2 | HG01255.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.1789-622_1789-613d others(12): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170123356 | ||||||
| chr3:170123356
|
T | TACACACA others(5): Show |
108 | a0001c0001t0002g0121a0001c0001t0002g0123a0001c0001t0002g0124others(105): Show | 110 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.1789-624_1789-613d others(14): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170123356 | ||||||
| chr3:170123356
|
T | TACACACA others(7): Show |
27 | a0001c0001t0002g0118a0001c0001t0002g0180a0001c0001t0002g0289others(24): Show | 27 | HG00140.hp1 HG00639.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.1789-626_1789-613d others(16): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170123356 | ||||||
| chr3:170123356
|
T | TACACACA others(9): Show |
8 | a0001c0001t0006g0004a0001c0001t0006g0189a0001c0001t0006g0190others(5): Show | 8 | HG02109.hp1 HG02630.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.1789-628_1789-613d others(18): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170123356 | ||||||
| chr3:170123356
|
T | TACACACA others(11): Show |
59 | a0001c0001t0002g0272a0001c0001t0004g0005a0001c0001t0004g0006others(56): Show | 59 | HG00558.hp1 HG00597.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.1789-630_1789-613d others(20): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170123356 | ||||||
| chr3:170123356
|
T | TACACACA others(13): Show |
19 | a0001c0001t0004g0127a0001c0001t0004g0165a0001c0001t0004g0174others(16): Show | 20 | HG00408.hp1 HG00423.hp1 HG00673.hp2 others(17): Show |
intron_variant | MODIFIER | c.1789-613_1789-612i others(22): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170123356 | ||||||
| chr3:170123356
|
T | TACACACA others(15): Show |
1 | a0003c0005t0028g0325 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1789-613_1789-612i others(24): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170123356 | ||||||
| chr3:170123356
|
T | TACACACA others(19): Show |
1 | a0010c0007t0029g0323 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1789-613_1789-612i others(28): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170123356 | ||||||
| chr3:170123645
|
T | C | 1 | a0001c0001t0041g0207 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1789-901A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170123645 | ||||||
| chr3:170123772
|
A | G | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1789-1028T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170123772 | ||||||
| chr3:170123836
|
G | A | 6 | a0001c0001t0010g0028a0001c0001t0010g0029a0001c0001t0014g0109others(3): Show | 6 | HG02257.hp2 HG02615.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1789-1092C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170123836 | ||||||
| chr3:170123918
|
C | A | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1789-1174G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170123918 | ||||||
| chr3:170124138
|
G | A | 54 | a0001c0001t0004g0005a0001c0001t0004g0006a0001c0001t0004g0127others(51): Show | 55 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.1789-1394C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170124138 | ||||||
| chr3:170124196
|
G | T | 1 | a0001c0001t0003g0204 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1789-1452C>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170124196 | ||||||
| chr3:170124439
|
G | A | 6 | a0001c0001t0002g0129a0001c0001t0002g0181a0001c0001t0002g0219others(3): Show | 6 | HG01943.hp2 HG01981.hp1 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.1789-1695C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170124439 | ||||||
| chr3:170124493
|
G | A | 1 | a0001c0001t0001g0059 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1789-1749C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170124493 | ||||||
| chr3:170124838
|
A | G | 10 | a0001c0001t0003g0257a0001c0001t0003g0258a0001c0001t0003g0259others(7): Show | 10 | HG01175.hp1 HG01255.hp2 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.1789-2094T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170124838 | ||||||
| chr3:170125007
|
G | A | 1 | a0001c0001t0003g0199 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1789-2263C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170125007 | ||||||
| chr3:170125130
|
G | A | 1 | a0001c0001t0002g0247 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1789-2386C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170125130 | ||||||
| chr3:170125130
|
G | T | 4 | a0001c0001t0003g0179a0001c0001t0003g0209a0001c0001t0003g0210others(1): Show | 4 | HG02145.hp1 HG02970.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1789-2386C>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170125130 | ||||||
| chr3:170125380
|
T | C | 101 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(98): Show | 102 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.1789-2636A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170125380 | ||||||
| chr3:170125400
|
T | C | 1 | a0001c0001t0002g0275 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1789-2656A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170125400 | ||||||
| chr3:170125589
|
AT | A | 2 | a0001c0001t0007g0003a0001c0001t0007g0152 | 3 | HG01257.hp1 HG01346.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.1789-2846delA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170125589 | ||||||
| chr3:170125636
|
C | T | 1 | a0001c0001t0003g0260 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1789-2892G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170125636 | ||||||
| chr3:170125643
|
A | G | 1 | a0001c0001t0004g0161 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1789-2899T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170125643 | ||||||
| chr3:170125924
|
A | G | 19 | a0001c0002t0005g0305a0001c0002t0005g0306a0001c0002t0005g0307others(16): Show | 19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.1788+2760T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170125924 | ||||||
| chr3:170125925
|
TA | T | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1788+2758delT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170125925 | ||||||
| chr3:170126053
|
T | A | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1788+2631A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126053 | ||||||
| chr3:170126065
|
A | C | 1 | a0001c0001t0002g0222 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1788+2619T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126065 | ||||||
| chr3:170126394
|
G | A | 6 | a0001c0001t0012g0100a0001c0001t0012g0102a0001c0001t0012g0103others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1788+2290C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126394 | ||||||
| chr3:170126468
|
T | C | 1 | a0001c0001t0025g0253 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1788+2216A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126468 | ||||||
| chr3:170126504
|
G | GTA | 11 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0112others(8): Show | 11 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(8): Show |
intron_variant | MODIFIER | c.1788+2178_1788+217 others(6): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126504 | ||||||
| chr3:170126504
|
G | GTATA | 4 | a0001c0001t0001g0022a0001c0001t0001g0044a0001c0001t0034g0089others(1): Show | 4 | HG00558.hp2 NA18946.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.1788+2176_1788+217 others(8): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126504 | ||||||
| chr3:170126504
|
G | GTATATAT others(21): Show |
2 | a0001c0001t0014g0109a0001c0001t0014g0110 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1788+2179_1788+218 others(32): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126504 | ||||||
| chr3:170126504
|
G | GTGTATAT others(17): Show |
1 | a0001c0001t0045g0101 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1788+2179_1788+218 others(28): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126504 | ||||||
| chr3:170126504
|
GTA | G | 15 | a0001c0001t0003g0188a0001c0001t0003g0227a0001c0001t0003g0228others(12): Show | 15 | HG00140.hp1 HG01081.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.1788+2178_1788+217 others(6): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126504 | ||||||
| chr3:170126506
|
A | G | 7 | a0001c0001t0012g0100a0001c0001t0012g0102a0001c0001t0012g0103others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.1788+2178T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126506 | ||||||
| chr3:170126508
|
A | G | 1 | a0001c0001t0003g0257 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1788+2176T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126508 | ||||||
| chr3:170126510
|
A | G | 1 | a0010c0007t0029g0323 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1788+2174T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126510 | ||||||
| chr3:170126524
|
A | T | 1 | a0001c0001t0035g0304 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1788+2160T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126524 | ||||||
| chr3:170126525
|
TA | T | 14 | a0001c0001t0003g0258a0001c0001t0003g0259a0001c0001t0003g0261others(11): Show | 14 | HG01256.hp1 HG01258.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1788+2158delT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126525 | ||||||
| chr3:170126526
|
A | T | 3 | a0001c0001t0006g0279a0001c0001t0006g0280a0001c0001t0035g0304 | 3 | HG00642.hp1 HG01884.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1788+2158T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126526 | ||||||
| chr3:170126527
|
TA | T | 34 | a0001c0001t0002g0235a0001c0001t0002g0242a0001c0001t0003g0264others(31): Show | 35 | HG00639.hp2 HG00642.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.1788+2156delT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126527 | ||||||
| chr3:170126528
|
A | AT | 15 | a0001c0001t0001g0015a0001c0001t0001g0057a0001c0001t0002g0130others(12): Show | 15 | HG00408.hp2 HG01175.hp1 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.1788+2155dupA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126528 | ||||||
| chr3:170126528
|
A | ATAT | 16 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(13): Show | 16 | HG00544.hp2 HG00597.hp2 HG00621.hp2 others(13): Show |
intron_variant | MODIFIER | c.1788+2155_1788+215 others(7): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126528 | ||||||
| chr3:170126528
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0037g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1788+2155_1788+215 others(17): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126528 | ||||||
| chr3:170126528
|
A | ATATATAT others(20): Show |
3 | a0001c0001t0012g0102a0001c0001t0012g0103a0001c0001t0012g0104 | 3 | HG01167.hp1 HG01169.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1788+2155_1788+215 others(31): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126528 | ||||||
| chr3:170126528
|
A | ATATATAT others(21): Show |
1 | a0001c0001t0014g0111 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1788+2155_1788+215 others(32): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126528 | ||||||
| chr3:170126528
|
A | ATATATAT others(26): Show |
1 | a0001c0001t0010g0028 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1788+2155_1788+215 others(37): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126528 | ||||||
| chr3:170126528
|
A | ATATATAT others(32): Show |
1 | a0001c0001t0043g0030 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1788+2155_1788+215 others(43): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126528 | ||||||
| chr3:170126528
|
A | ATATATAT others(5): Show |
1 | a0001c0001t0042g0194 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1788+2155_1788+215 others(16): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126528 | ||||||
| chr3:170126528
|
A | ATATT | 8 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(5): Show | 8 | HG01106.hp2 HG01256.hp2 HG03239.hp1 others(5): Show |
intron_variant | MODIFIER | c.1788+2155_1788+215 others(8): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126528 | ||||||
| chr3:170126528
|
A | ATT | 24 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0039others(21): Show | 24 | HG00673.hp1 HG01123.hp2 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.1788+2154_1788+215 others(6): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126528 | ||||||
| chr3:170126528
|
A | ATTT | 32 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0031others(29): Show | 33 | HG00280.hp1 HG00438.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.1788+2153_1788+215 others(7): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126528 | ||||||
| chr3:170126528
|
A | T | 30 | a0001c0001t0001g0049a0001c0001t0001g0054a0001c0001t0001g0092others(27): Show | 30 | HG00642.hp1 HG01081.hp2 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.1788+2156T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126528 | ||||||
| chr3:170126528
|
AT | A | 70 | a0001c0001t0002g0118a0001c0001t0002g0121a0001c0001t0002g0123others(67): Show | 70 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.1788+2155delA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126528 | ||||||
| chr3:170126529
|
T | TA | 18 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0002g0247others(15): Show | 18 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.1788+2154_1788+215 others(5): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126529 | ||||||
| chr3:170126529
|
T | TATATATA others(4): Show |
1 | a0001c0001t0054g0105 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1788+2154_1788+215 others(15): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126529 | ||||||
| chr3:170126529
|
T | TATATATA others(10): Show |
1 | a0001c0001t0012g0100 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1788+2154_1788+215 others(21): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126529 | ||||||
| chr3:170126530
|
T | A | 19 | a0001c0001t0002g0285a0001c0001t0003g0119a0001c0001t0003g0203others(16): Show | 19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.1788+2154A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126530 | ||||||
| chr3:170126531
|
T | A | 20 | a0001c0001t0002g0123a0001c0001t0002g0129a0001c0001t0002g0131others(17): Show | 20 | HG00140.hp2 HG00280.hp2 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.1788+2153A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126531 | ||||||
| chr3:170126533
|
T | A | 2 | a0001c0001t0003g0179a0001c0001t0003g0211 | 2 | HG02145.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1788+2151A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126533 | ||||||
| chr3:170126742
|
T | C | 1 | a0005c0011t0002g0237 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1788+1942A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126742 | ||||||
| chr3:170126929
|
TG | T | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1788+1754delC | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126929 | ||||||
| chr3:170126930
|
G | T | 80 | a0001c0001t0004g0005a0001c0001t0004g0006a0001c0001t0004g0127others(77): Show | 81 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.1788+1754C>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126930 | ||||||
| chr3:170126953
|
A | T | 1 | a0011c0006t0002g0122 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1788+1731T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170126953 | ||||||
| chr3:170127019
|
T | C | 2 | a0001c0001t0031g0114a0001c0001t0032g0115 | 2 | HG00639.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1788+1665A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170127019 | ||||||
| chr3:170127086
|
T | A | 192 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(189): Show | 194 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1788+1598A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170127086 | ||||||
| chr3:170127136
|
A | C | 1 | a0001c0001t0003g0203 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1788+1548T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170127136 | ||||||
| chr3:170127145
|
T | C | 147 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(144): Show | 149 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.1788+1539A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170127145 | ||||||
| chr3:170127166
|
A | T | 19 | a0001c0002t0005g0305a0001c0002t0005g0306a0001c0002t0005g0307others(16): Show | 19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.1788+1518T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170127166 | ||||||
| chr3:170127234
|
T | G | 3 | a0001c0001t0007g0149a0001c0001t0018g0170a0006c0008t0018g0150 | 3 | HG02622.hp1 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1788+1450A>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170127234 | ||||||
| chr3:170127339
|
T | C | 19 | a0001c0002t0005g0305a0001c0002t0005g0306a0001c0002t0005g0307others(16): Show | 19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.1788+1345A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170127339 | ||||||
| chr3:170127382
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1788+1302C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170127382 | ||||||
| chr3:170127386
|
C | A | 1 | a0001c0001t0003g0262 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1788+1298G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170127386 | ||||||
| chr3:170127497
|
G | A | 18 | a0001c0001t0010g0028a0001c0001t0010g0029a0001c0001t0012g0100others(15): Show | 18 | HG00639.hp1 HG01167.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.1788+1187C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170127497 | ||||||
| chr3:170127512
|
C | CTT | 192 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(189): Show | 194 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1788+1171_1788+117 others(6): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170127512 | ||||||
| chr3:170127711
|
G | C | 1 | a0001c0001t0003g0208 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1788+973C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170127711 | ||||||
| chr3:170127816
|
T | G | 46 | a0001c0001t0004g0005a0001c0001t0004g0006a0001c0001t0004g0127others(43): Show | 47 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.1788+868A>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170127816 | ||||||
| chr3:170128097
|
C | A | 5 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0002g0247others(2): Show | 5 | NA18943.hp2 NA18944.hp2 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.1788+587G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170128097 | ||||||
| chr3:170128097
|
C | T | 1 | a0001c0001t0011g0098 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1788+587G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170128097 | ||||||
| chr3:170128234
|
A | C | 5 | a0001c0001t0002g0118a0001c0001t0002g0289a0001c0001t0033g0239others(2): Show | 5 | HG02132.hp1 NA18959.hp2 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.1788+450T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170128234 | ||||||
| chr3:170128270
|
G | C | 1 | a0001c0001t0001g0086 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1788+414C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170128270 | ||||||
| chr3:170128272
|
T | A | 1 | a0001c0001t0001g0086 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1788+412A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170128272 | ||||||
| chr3:170128290
|
C | T | 1 | a0001c0001t0002g0281 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1788+394G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 8/14 | chr3 | 170128290 | ||||||
| chr3:170129705
|
A | T | 1 | a0001c0001t0002g0185 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.920-153T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170129705 | ||||||
| chr3:170129787
|
C | T | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.920-235G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170129787 | ||||||
| chr3:170129841
|
A | C | 1 | a0001c0001t0008g0177 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.920-289T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170129841 | ||||||
| chr3:170129866
|
A | T | 101 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(98): Show | 102 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.920-314T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170129866 | ||||||
| chr3:170129889
|
G | A | 3 | a0001c0001t0014g0109a0001c0001t0014g0110a0001c0001t0014g0111 | 3 | HG02257.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.920-337C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170129889 | ||||||
| chr3:170129901
|
C | T | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.920-349G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170129901 | ||||||
| chr3:170129990
|
C | T | 1 | a0001c0001t0007g0142 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.920-438G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170129990 | ||||||
| chr3:170130039
|
T | C | 1 | a0010c0007t0029g0323 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.920-487A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170130039 | ||||||
| chr3:170130069
|
T | G | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.920-517A>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170130069 | ||||||
| chr3:170130214
|
T | C | 2 | a0001c0001t0031g0114a0001c0001t0032g0115 | 2 | HG00639.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.920-662A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170130214 | ||||||
| chr3:170130292
|
G | A | 1 | a0001c0001t0002g0284 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.920-740C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170130292 | ||||||
| chr3:170130399
|
T | C | 1 | a0001c0001t0033g0239 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.920-847A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170130399 | ||||||
| chr3:170130514
|
A | C | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.920-962T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170130514 | ||||||
| chr3:170130566
|
T | C | 1 | a0001c0001t0001g0031 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.920-1014A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170130566 | ||||||
| chr3:170130602
|
AT | A | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.920-1051delA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170130602 | ||||||
| chr3:170130884
|
A | G | 1 | a0003c0005t0027g0324 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.920-1332T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170130884 | ||||||
| chr3:170130943
|
G | GA | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.920-1392dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170130943 | ||||||
| chr3:170131002
|
A | G | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.920-1450T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170131002 | ||||||
| chr3:170131116
|
G | A | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.920-1564C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170131116 | ||||||
| chr3:170131145
|
TA | T | 200 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(197): Show | 203 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.920-1594delT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170131145 | ||||||
| chr3:170131145
|
TAA | T | 96 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0045others(93): Show | 97 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.920-1595_920-1594d others(4): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170131145 | ||||||
| chr3:170131148
|
A | T | 18 | a0001c0002t0005g0305a0001c0002t0005g0306a0001c0002t0005g0307others(15): Show | 18 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(15): Show |
intron_variant | MODIFIER | c.920-1596T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170131148 | ||||||
| chr3:170131149
|
A | T | 1 | a0001c0002t0005g0308 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.920-1597T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170131149 | ||||||
| chr3:170131194
|
TA | T | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.920-1643delT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170131194 | ||||||
| chr3:170131299
|
T | TAACAAAA others(363): Show |
1 | a0001c0001t0010g0020 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.920-1748_920-1747i others(372): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170131299 | ||||||
| chr3:170131308
|
C | A | 8 | a0001c0001t0008g0113a0001c0001t0008g0116a0001c0001t0008g0117others(5): Show | 8 | HG02055.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.920-1756G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170131308 | ||||||
| chr3:170131324
|
G | A | 2 | a0001c0001t0016g0206a0001c0001t0016g0282 | 2 | HG01884.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.920-1772C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170131324 | ||||||
| chr3:170131618
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.920-2066C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170131618 | ||||||
| chr3:170131691
|
G | A | 6 | a0001c0001t0012g0100a0001c0001t0012g0102a0001c0001t0012g0103others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.920-2139C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170131691 | ||||||
| chr3:170131735
|
G | A | 1 | a0001c0001t0056g0160 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.920-2183C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170131735 | ||||||
| chr3:170131963
|
G | A | 1 | a0001c0001t0041g0207 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.920-2411C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170131963 | ||||||
| chr3:170131974
|
G | C | 5 | a0001c0001t0015g0254a0001c0001t0015g0255a0001c0001t0015g0256others(2): Show | 7 | HG01243.hp1 HG02258.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.920-2422C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170131974 | ||||||
| chr3:170132082
|
G | A | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.920-2530C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170132082 | ||||||
| chr3:170132082
|
G | GA | 19 | a0001c0002t0005g0305a0001c0002t0005g0306a0001c0002t0005g0307others(16): Show | 19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.920-2531dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170132082 | ||||||
| chr3:170132183
|
CAT | C | 19 | a0001c0002t0005g0305a0001c0002t0005g0306a0001c0002t0005g0307others(16): Show | 19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.920-2633_920-2632d others(4): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170132183 | ||||||
| chr3:170132301
|
G | C | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.920-2749C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170132301 | ||||||
| chr3:170132392
|
C | T | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.920-2840G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170132392 | ||||||
| chr3:170132524
|
A | C | 1 | a0001c0001t0037g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.920-2972T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170132524 | ||||||
| chr3:170132660
|
G | A | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.920-3108C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170132660 | ||||||
| chr3:170132709
|
C | G | 3 | a0001c0001t0001g0018a0001c0001t0001g0027a0001c0001t0001g0120 | 3 | NA18992.hp1 NA19066.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.920-3157G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170132709 | ||||||
| chr3:170132748
|
G | A | 7 | a0001c0002t0005g0305a0001c0002t0005g0311a0001c0002t0005g0312others(4): Show | 7 | HG00408.hp1 HG00423.hp1 HG00673.hp2 others(4): Show |
intron_variant | MODIFIER | c.920-3196C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170132748 | ||||||
| chr3:170132839
|
A | C | 1 | a0001c0001t0040g0048 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.920-3287T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170132839 | ||||||
| chr3:170133112
|
A | T | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.919+3307T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170133112 | ||||||
| chr3:170133159
|
A | G | 1 | a0001c0001t0011g0065 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.919+3260T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170133159 | ||||||
| chr3:170133182
|
CT | C | 9 | a0001c0001t0008g0113a0001c0001t0008g0116a0001c0001t0008g0117others(6): Show | 9 | HG02055.hp2 HG02622.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.919+3236delA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170133182 | ||||||
| chr3:170133323
|
A | C | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.919+3096T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170133323 | ||||||
| chr3:170133368
|
G | A | 2 | a0001c0001t0002g0223a0001c0001t0002g0278 | 2 | HG03490.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.919+3051C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170133368 | ||||||
| chr3:170133384
|
G | C | 1 | a0001c0002t0005g0310 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.919+3035C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170133384 | ||||||
| chr3:170133441
|
T | C | 1 | a0001c0001t0037g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.919+2978A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170133441 | ||||||
| chr3:170133651
|
T | C | 1 | a0001c0001t0001g0090 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.919+2768A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170133651 | ||||||
| chr3:170133803
|
G | A | 3 | a0001c0001t0008g0113a0001c0001t0008g0116a0001c0001t0008g0117 | 3 | HG02622.hp2 HG02818.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.919+2616C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170133803 | ||||||
| chr3:170133817
|
A | T | 67 | a0001c0001t0002g0118a0001c0001t0002g0121a0001c0001t0002g0123others(64): Show | 67 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.919+2602T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170133817 | ||||||
| chr3:170133864
|
C | T | 2 | a0001c0001t0031g0114a0001c0001t0032g0115 | 2 | HG00639.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.919+2555G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170133864 | ||||||
| chr3:170134079
|
C | T | 1 | a0001c0001t0051g0245 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.919+2340G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170134079 | ||||||
| chr3:170134379
|
G | A | 1 | a0001c0001t0011g0291 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.919+2040C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170134379 | ||||||
| chr3:170134512
|
C | T | 7 | a0001c0003t0006g0293a0001c0003t0006g0294a0001c0003t0006g0295others(4): Show | 7 | HG01433.hp1 HG02055.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.919+1907G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170134512 | ||||||
| chr3:170135082
|
T | C | 1 | a0001c0001t0001g0034 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.919+1337A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170135082 | ||||||
| chr3:170135111
|
C | T | 19 | a0001c0002t0005g0305a0001c0002t0005g0306a0001c0002t0005g0307others(16): Show | 19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.919+1308G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170135111 | ||||||
| chr3:170135137
|
T | A | 1 | a0001c0001t0002g0248 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.919+1282A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170135137 | ||||||
| chr3:170135139
|
TTTTG | T | 7 | a0001c0001t0003g0179a0001c0001t0003g0209a0001c0001t0003g0210others(4): Show | 7 | HG02145.hp1 HG02630.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.919+1276_919+1279d others(6): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170135139 | ||||||
| chr3:170135139
|
TTTTGTTT others(1): Show |
T | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.919+1272_919+1279d others(10): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170135139 | ||||||
| chr3:170135253
|
T | C | 1 | a0001c0001t0048g0297 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.919+1166A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170135253 | ||||||
| chr3:170135343
|
T | G | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.919+1076A>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170135343 | ||||||
| chr3:170135421
|
G | A | 15 | a0001c0001t0010g0028a0001c0001t0010g0029a0001c0001t0012g0100others(12): Show | 15 | HG00639.hp1 HG01167.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.919+998C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170135421 | ||||||
| chr3:170135453
|
A | AT | 101 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(98): Show | 102 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.919+965dupA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170135453 | ||||||
| chr3:170135488
|
A | T | 1 | a0001c0001t0031g0114 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.919+931T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170135488 | ||||||
| chr3:170135506
|
T | TA | 15 | a0001c0001t0010g0028a0001c0001t0010g0029a0001c0001t0012g0100others(12): Show | 15 | HG00639.hp1 HG01167.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.919+912dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170135506 | ||||||
| chr3:170135512
|
T | TACACAC | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.919+901_919+906dup others(6): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170135512 | ||||||
| chr3:170135654
|
TACTA | T | 15 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(12): Show | 15 | HG00544.hp2 HG00558.hp2 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.919+761_919+764del others(4): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170135654 | ||||||
| chr3:170135747
|
CT | C | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.919+671delA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170135747 | ||||||
| chr3:170135808
|
A | G | 19 | a0001c0002t0005g0305a0001c0002t0005g0306a0001c0002t0005g0307others(16): Show | 19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.919+611T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170135808 | ||||||
| chr3:170135851
|
G | C | 1 | a0001c0001t0022g0007 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.919+568C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170135851 | ||||||
| chr3:170135975
|
GACA | G | 15 | a0001c0001t0010g0028a0001c0001t0010g0029a0001c0001t0012g0100others(12): Show | 15 | HG00639.hp1 HG01167.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.919+441_919+443del others(3): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170135975 | ||||||
| chr3:170136031
|
T | G | 1 | a0001c0001t0002g0180 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.919+388A>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170136031 | ||||||
| chr3:170136155
|
T | C | 1 | a0001c0001t0006g0191 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.919+264A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170136155 | ||||||
| chr3:170136210
|
A | T | 2 | a0001c0001t0002g0131a0001c0001t0002g0215 | 2 | HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.919+209T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170136210 | ||||||
| chr3:170136252
|
CT | C | 3 | a0002c0004t0017g0062a0002c0004t0017g0063a0002c0004t0017g0196 | 3 | HG02615.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.919+166delA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170136252 | ||||||
| chr3:170136289
|
G | A | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.919+130C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170136289 | ||||||
| chr3:170136413
|
T | A | 2 | a0001c0001t0001g0040a0001c0001t0001g0042 | 2 | NA18940.hp1 NA19091.hp1 |
splice_region_variant&intron_variant | LOW | c.919+6A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 7/14 | chr3 | 170136413 | ||||||
| chr3:170136796
|
A | G | 1 | a0001c0001t0001g0021 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.673-131T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170136796 | ||||||
| chr3:170136808
|
A | G | 1 | a0001c0001t0004g0159 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.673-143T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170136808 | ||||||
| chr3:170136883
|
T | C | 155 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(152): Show | 157 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.673-218A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170136883 | ||||||
| chr3:170136977
|
A | G | 5 | a0001c0001t0008g0113a0001c0001t0008g0116a0001c0001t0008g0117others(2): Show | 5 | HG02055.hp2 HG02622.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.673-312T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170136977 | ||||||
| chr3:170137208
|
G | GT | 19 | a0001c0002t0005g0305a0001c0002t0005g0306a0001c0002t0005g0307others(16): Show | 19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.673-544dupA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170137208 | ||||||
| chr3:170137438
|
G | T | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.673-773C>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170137438 | ||||||
| chr3:170137450
|
G | A | 1 | a0001c0001t0003g0200 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.673-785C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170137450 | ||||||
| chr3:170137562
|
A | G | 1 | a0001c0001t0003g0260 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.673-897T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170137562 | ||||||
| chr3:170137641
|
C | T | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.673-976G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170137641 | ||||||
| chr3:170138152
|
G | A | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.673-1487C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170138152 | ||||||
| chr3:170138227
|
A | T | 2 | a0001c0001t0004g0154a0001c0001t0004g0162 | 2 | NA18943.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.673-1562T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170138227 | ||||||
| chr3:170138306
|
G | A | 6 | a0001c0001t0003g0257a0001c0001t0003g0258a0001c0001t0003g0259others(3): Show | 6 | HG02486.hp1 HG02559.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.673-1641C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170138306 | ||||||
| chr3:170138412
|
C | A | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.673-1747G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170138412 | ||||||
| chr3:170138539
|
AATTAGCC others(2): Show |
A | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.673-1883_673-1875d others(11): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170138539 | ||||||
| chr3:170138586
|
A | G | 1 | a0001c0001t0001g0010 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.673-1921T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170138586 | ||||||
| chr3:170138597
|
G | A | 1 | a0001c0002t0005g0307 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.673-1932C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170138597 | ||||||
| chr3:170138689
|
C | CA | 15 | a0001c0001t0002g0130a0001c0001t0002g0184a0001c0001t0002g0185others(12): Show | 15 | HG00609.hp1 HG02040.hp1 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.673-2025dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170138689 | ||||||
| chr3:170138689
|
CA | C | 173 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(170): Show | 175 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.673-2025delT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170138689 | ||||||
| chr3:170138689
|
CAA | C | 13 | a0001c0001t0004g0163a0001c0001t0006g0189a0001c0001t0011g0065others(10): Show | 13 | HG00438.hp1 HG01433.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.673-2026_673-2025d others(4): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170138689 | ||||||
| chr3:170138776
|
G | A | 1 | a0001c0001t0054g0105 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.673-2111C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170138776 | ||||||
| chr3:170138886
|
A | C | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.673-2221T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170138886 | ||||||
| chr3:170138915
|
A | C | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.673-2250T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170138915 | ||||||
| chr3:170138965
|
T | C | 2 | a0001c0001t0001g0106a0001c0001t0001g0290 | 2 | HG02056.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.673-2300A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170138965 | ||||||
| chr3:170139000
|
G | A | 1 | a0001c0001t0016g0205 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.673-2335C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170139000 | ||||||
| chr3:170139189
|
A | G | 7 | a0001c0001t0008g0113a0001c0001t0008g0116a0001c0001t0008g0117others(4): Show | 7 | HG00639.hp1 HG02055.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.673-2524T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170139189 | ||||||
| chr3:170139199
|
G | GACTTAAT others(3): Show |
1 | a0001c0001t0001g0021 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.673-2535_673-2534i others(12): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170139199 | ||||||
| chr3:170139201
|
T | G | 1 | a0001c0001t0001g0021 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.673-2536A>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170139201 | ||||||
| chr3:170139202
|
C | A | 1 | a0001c0001t0001g0021 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.673-2537G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170139202 | ||||||
| chr3:170139219
|
C | T | 308 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(305): Show | 312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.673-2554G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170139219 | ||||||
| chr3:170139564
|
G | C | 1 | a0001c0001t0001g0010 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.673-2899C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170139564 | ||||||
| chr3:170139702
|
T | C | 1 | a0001c0001t0001g0078 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.673-3037A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170139702 | ||||||
| chr3:170140216
|
T | C | 7 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0044others(4): Show | 7 | HG01433.hp2 HG02300.hp1 NA18957.hp1 others(4): Show |
intron_variant | MODIFIER | c.673-3551A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170140216 | ||||||
| chr3:170140222
|
A | G | 1 | a0007c0009t0001g0019 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.673-3557T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170140222 | ||||||
| chr3:170140440
|
G | A | 46 | a0001c0001t0004g0005a0001c0001t0004g0006a0001c0001t0004g0127others(43): Show | 47 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.673-3775C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170140440 | ||||||
| chr3:170140451
|
G | A | 3 | a0001c0001t0003g0262a0001c0001t0003g0263a0001c0001t0003g0265 | 3 | HG01175.hp1 HG01934.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.673-3786C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170140451 | ||||||
| chr3:170140582
|
T | C | 1 | a0001c0001t0003g0232 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.673-3917A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170140582 | ||||||
| chr3:170140584
|
C | CT | 34 | a0001c0001t0001g0025a0001c0001t0002g0186a0001c0001t0002g0192others(31): Show | 34 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.673-3920dupA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170140584 | ||||||
| chr3:170140584
|
CT | C | 96 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(93): Show | 97 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.673-3920delA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170140584 | ||||||
| chr3:170140584
|
CTT | C | 12 | a0001c0001t0001g0037a0001c0001t0001g0084a0001c0001t0001g0106others(9): Show | 12 | HG00639.hp1 HG01256.hp2 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.673-3921_673-3920d others(4): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170140584 | ||||||
| chr3:170140584
|
CTTTTTTT others(6): Show |
C | 2 | a0001c0001t0002g0214a0001c0001t0002g0286 | 2 | HG00609.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.673-3932_673-3920d others(15): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170140584 | ||||||
| chr3:170140587
|
T | C | 7 | a0001c0001t0006g0004a0001c0001t0006g0141a0001c0001t0006g0189others(4): Show | 7 | HG01884.hp1 HG02109.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.673-3922A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170140587 | ||||||
| chr3:170140619
|
A | T | 1 | a0001c0001t0001g0054 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.673-3954T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170140619 | ||||||
| chr3:170140627
|
C | T | 308 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(305): Show | 312 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(309): Show |
intron_variant | MODIFIER | c.673-3962G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170140627 | ||||||
| chr3:170140645
|
C | G | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.673-3980G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170140645 | ||||||
| chr3:170140650
|
G | A | 1 | a0001c0001t0037g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.673-3985C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170140650 | ||||||
| chr3:170140687
|
G | A | 1 | a0001c0001t0003g0262 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.673-4022C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170140687 | ||||||
| chr3:170140703
|
C | T | 1 | a0001c0001t0042g0194 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.673-4038G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170140703 | ||||||
| chr3:170140730
|
G | A | 1 | a0001c0001t0003g0262 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.673-4065C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170140730 | ||||||
| chr3:170140925
|
C | T | 1 | a0006c0008t0018g0150 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.673-4260G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170140925 | ||||||
| chr3:170141015
|
A | G | 2 | a0001c0001t0007g0003a0001c0001t0007g0152 | 3 | HG01257.hp1 HG01346.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.673-4350T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170141015 | ||||||
| chr3:170141286
|
T | C | 5 | a0001c0001t0015g0254a0001c0001t0015g0255a0001c0001t0015g0256others(2): Show | 7 | HG01243.hp1 HG02258.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.672+4137A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170141286 | ||||||
| chr3:170141370
|
C | G | 5 | a0001c0001t0015g0254a0001c0001t0015g0255a0001c0001t0015g0256others(2): Show | 7 | HG01243.hp1 HG02258.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.672+4053G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170141370 | ||||||
| chr3:170141505
|
T | C | 1 | a0001c0001t0031g0114 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.672+3918A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170141505 | ||||||
| chr3:170141768
|
C | T | 1 | a0001c0001t0004g0166 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.672+3655G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170141768 | ||||||
| chr3:170141792
|
T | C | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.672+3631A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170141792 | ||||||
| chr3:170141902
|
C | G | 4 | a0001c0001t0003g0119a0001c0001t0003g0197a0001c0001t0003g0201others(1): Show | 4 | HG00438.hp2 NA18959.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.672+3521G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170141902 | ||||||
| chr3:170142082
|
T | C | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.672+3341A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170142082 | ||||||
| chr3:170142099
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.672+3324G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170142099 | ||||||
| chr3:170142451
|
C | T | 49 | a0001c0001t0004g0005a0001c0001t0004g0006a0001c0001t0004g0127others(46): Show | 50 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.672+2972G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170142451 | ||||||
| chr3:170142661
|
G | T | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.672+2762C>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170142661 | ||||||
| chr3:170142744
|
T | C | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.672+2679A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170142744 | ||||||
| chr3:170142912
|
A | G | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.672+2511T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170142912 | ||||||
| chr3:170143378
|
A | T | 19 | a0001c0002t0005g0305a0001c0002t0005g0306a0001c0002t0005g0307others(16): Show | 19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.672+2045T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170143378 | ||||||
| chr3:170143505
|
AT | A | 19 | a0001c0001t0003g0119a0001c0001t0003g0179a0001c0001t0003g0197others(16): Show | 19 | HG00438.hp2 HG01884.hp2 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.672+1917delA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170143505 | ||||||
| chr3:170143533
|
A | G | 19 | a0001c0002t0005g0305a0001c0002t0005g0306a0001c0002t0005g0307others(16): Show | 19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.672+1890T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170143533 | ||||||
| chr3:170143570
|
C | T | 194 | a0001c0001t0002g0118a0001c0001t0002g0121a0001c0001t0002g0123others(191): Show | 197 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.672+1853G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170143570 | ||||||
| chr3:170143804
|
T | C | 1 | a0010c0007t0029g0323 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.672+1619A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170143804 | ||||||
| chr3:170143807
|
T | C | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.672+1616A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170143807 | ||||||
| chr3:170143969
|
G | C | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.672+1454C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170143969 | ||||||
| chr3:170143993
|
T | C | 3 | a0001c0001t0008g0175a0001c0001t0008g0176a0001c0001t0008g0177 | 3 | HG02630.hp2 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.672+1430A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170143993 | ||||||
| chr3:170144145
|
C | G | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.672+1278G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170144145 | ||||||
| chr3:170144158
|
T | TA | 56 | a0001c0001t0001g0106a0001c0001t0001g0290a0001c0001t0004g0005others(53): Show | 57 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.672+1264dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170144158 | ||||||
| chr3:170144159
|
A | C | 1 | a0003c0005t0027g0324 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.672+1264T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170144159 | ||||||
| chr3:170144169
|
A | G | 1 | a0001c0001t0001g0303 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.672+1254T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170144169 | ||||||
| chr3:170144201
|
C | T | 1 | a0001c0001t0038g0024 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.672+1222G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170144201 | ||||||
| chr3:170144202
|
G | A | 7 | a0001c0001t0008g0113a0001c0001t0008g0116a0001c0001t0008g0117others(4): Show | 7 | HG00639.hp1 HG02055.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.672+1221C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170144202 | ||||||
| chr3:170144297
|
T | C | 7 | a0001c0001t0008g0113a0001c0001t0008g0116a0001c0001t0008g0117others(4): Show | 7 | HG00639.hp1 HG02055.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.672+1126A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170144297 | ||||||
| chr3:170144308
|
T | C | 2 | a0003c0005t0027g0324a0003c0005t0028g0325 | 2 | HG01433.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.672+1115A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170144308 | ||||||
| chr3:170144341
|
CA | C | 6 | a0001c0001t0002g0275a0001c0001t0003g0268a0001c0001t0007g0195others(3): Show | 6 | HG00639.hp1 HG01168.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.672+1081delT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170144341 | ||||||
| chr3:170144478
|
G | A | 2 | a0002c0004t0017g0062a0002c0004t0017g0063 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.672+945C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170144478 | ||||||
| chr3:170144691
|
G | A | 1 | a0001c0001t0032g0115 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.672+732C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170144691 | ||||||
| chr3:170144711
|
T | C | 1 | a0010c0007t0029g0323 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.672+712A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170144711 | ||||||
| chr3:170144810
|
ATCC | A | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.672+610_672+612del others(3): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170144810 | ||||||
| chr3:170144896
|
C | T | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.672+527G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170144896 | ||||||
| chr3:170145042
|
C | A | 1 | a0001c0001t0007g0195 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.672+381G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170145042 | ||||||
| chr3:170145150
|
G | T | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.672+273C>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170145150 | ||||||
| chr3:170145346
|
A | C | 3 | a0001c0001t0008g0175a0001c0001t0008g0176a0001c0001t0008g0177 | 3 | HG02630.hp2 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.672+77T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 6/14 | chr3 | 170145346 | ||||||
| chr3:170145822
|
C | T | 1 | a0001c0002t0005g0322 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.574-301G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170145822 | ||||||
| chr3:170145879
|
G | GAAGTTA | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.574-359_574-358ins others(6): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170145879 | ||||||
| chr3:170146100
|
C | T | 3 | a0001c0001t0014g0109a0001c0001t0014g0110a0001c0001t0014g0111 | 3 | HG02257.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.574-579G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170146100 | ||||||
| chr3:170146101
|
G | A | 1 | a0001c0001t0003g0257 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.574-580C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170146101 | ||||||
| chr3:170146308
|
G | A | 49 | a0001c0001t0004g0005a0001c0001t0004g0006a0001c0001t0004g0127others(46): Show | 50 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.574-787C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170146308 | ||||||
| chr3:170146366
|
C | A | 49 | a0001c0001t0004g0005a0001c0001t0004g0006a0001c0001t0004g0127others(46): Show | 50 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.574-845G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170146366 | ||||||
| chr3:170146535
|
C | CT | 12 | a0001c0001t0002g0123a0001c0001t0002g0184a0001c0001t0002g0240others(9): Show | 12 | HG00280.hp2 HG01884.hp1 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.574-1015dupA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170146535 | ||||||
| chr3:170146535
|
CT | C | 162 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(159): Show | 164 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.574-1015delA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170146535 | ||||||
| chr3:170146767
|
A | C | 1 | a0001c0001t0001g0093 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.574-1246T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170146767 | ||||||
| chr3:170146869
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.574-1348A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170146869 | ||||||
| chr3:170146877
|
C | CT | 12 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0054others(9): Show | 12 | HG00735.hp1 HG00735.hp2 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.574-1357dupA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170146877 | ||||||
| chr3:170146877
|
CT | C | 30 | a0001c0001t0001g0037a0001c0001t0001g0041a0001c0001t0001g0094others(27): Show | 30 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.574-1357delA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170146877 | ||||||
| chr3:170146877
|
CTTTTTTT others(6): Show |
C | 3 | a0001c0001t0014g0109a0001c0001t0014g0110a0001c0001t0014g0111 | 3 | HG02257.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.574-1369_574-1357d others(15): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170146877 | ||||||
| chr3:170146943
|
C | A | 1 | a0001c0001t0003g0119 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.574-1422G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170146943 | ||||||
| chr3:170147096
|
C | T | 1 | a0001c0001t0042g0194 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.574-1575G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170147096 | ||||||
| chr3:170147278
|
T | C | 1 | a0001c0001t0037g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.574-1757A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170147278 | ||||||
| chr3:170147282
|
A | T | 1 | a0001c0001t0010g0095 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.574-1761T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170147282 | ||||||
| chr3:170147359
|
T | TA | 51 | a0001c0001t0004g0005a0001c0001t0004g0006a0001c0001t0004g0127others(48): Show | 52 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.573+1726dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170147359 | ||||||
| chr3:170147376
|
G | C | 5 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0002g0247others(2): Show | 5 | NA18943.hp2 NA18944.hp2 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.573+1710C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170147376 | ||||||
| chr3:170147554
|
CTTG | C | 3 | a0001c0001t0014g0109a0001c0001t0014g0110a0001c0001t0014g0111 | 3 | HG02257.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.573+1529_573+1531d others(5): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170147554 | ||||||
| chr3:170147631
|
C | T | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.573+1455G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170147631 | ||||||
| chr3:170147634
|
T | C | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.573+1452A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170147634 | ||||||
| chr3:170147863
|
C | T | 1 | a0001c0001t0002g0219 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.573+1223G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170147863 | ||||||
| chr3:170147950
|
T | C | 5 | a0001c0001t0008g0113a0001c0001t0008g0116a0001c0001t0008g0117others(2): Show | 5 | HG02055.hp2 HG02622.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.573+1136A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170147950 | ||||||
| chr3:170148061
|
G | A | 1 | a0001c0001t0002g0244 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.573+1025C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170148061 | ||||||
| chr3:170148121
|
T | C | 7 | a0001c0001t0008g0113a0001c0001t0008g0116a0001c0001t0008g0117others(4): Show | 7 | HG00639.hp1 HG02055.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.573+965A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170148121 | ||||||
| chr3:170148225
|
T | C | 194 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(191): Show | 196 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.573+861A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170148225 | ||||||
| chr3:170148226
|
G | A | 3 | a0001c0001t0014g0109a0001c0001t0014g0110a0001c0001t0014g0111 | 3 | HG02257.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.573+860C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170148226 | ||||||
| chr3:170148278
|
TAAC | T | 3 | a0001c0001t0008g0175a0001c0001t0008g0176a0001c0001t0008g0177 | 3 | HG02630.hp2 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.573+805_573+807del others(3): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170148278 | ||||||
| chr3:170148617
|
T | C | 1 | a0001c0001t0003g0134 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.573+469A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170148617 | ||||||
| chr3:170148836
|
C | G | 1 | a0001c0001t0001g0079 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.573+250G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170148836 | ||||||
| chr3:170148843
|
G | T | 1 | a0001c0001t0008g0176 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.573+243C>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170148843 | ||||||
| chr3:170148884
|
T | C | 1 | a0001c0001t0003g0267 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.573+202A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170148884 | ||||||
| chr3:170149008
|
CTT | C | 19 | a0001c0002t0005g0305a0001c0002t0005g0306a0001c0002t0005g0307others(16): Show | 19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.573+76_573+77delAA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170149008 | ||||||
| chr3:170149024
|
A | T | 19 | a0001c0001t0003g0119a0001c0001t0003g0179a0001c0001t0003g0197others(16): Show | 19 | HG00438.hp2 HG01884.hp2 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.573+62T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 5/14 | chr3 | 170149024 | ||||||
| chr3:170149472
|
A | C | 120 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(117): Show | 121 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.415-228T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170149472 | ||||||
| chr3:170149517
|
C | T | 1 | a0001c0001t0042g0194 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.415-273G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170149517 | ||||||
| chr3:170149529
|
A | G | 3 | a0001c0001t0010g0028a0001c0001t0010g0029a0001c0001t0043g0030 | 3 | HG02615.hp1 HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.415-285T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170149529 | ||||||
| chr3:170149608
|
C | T | 1 | a0001c0001t0009g0068 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.415-364G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170149608 | ||||||
| chr3:170149676
|
G | A | 43 | a0001c0001t0002g0131a0001c0001t0004g0005a0001c0001t0004g0006others(40): Show | 44 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.415-432C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170149676 | ||||||
| chr3:170149714
|
C | T | 1 | a0003c0005t0028g0325 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.415-470G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170149714 | ||||||
| chr3:170149778
|
A | G | 2 | a0001c0001t0001g0079a0001c0001t0026g0238 | 2 | HG02015.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.415-534T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170149778 | ||||||
| chr3:170149856
|
C | T | 7 | a0001c0001t0006g0004a0001c0001t0006g0141a0001c0001t0006g0189others(4): Show | 7 | HG01884.hp1 HG02109.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.415-612G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170149856 | ||||||
| chr3:170149956
|
A | G | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.415-712T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170149956 | ||||||
| chr3:170149985
|
A | G | 1 | a0001c0013t0002g0213 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.415-741T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170149985 | ||||||
| chr3:170150182
|
C | A | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.415-938G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170150182 | ||||||
| chr3:170150200
|
T | A | 1 | a0001c0002t0005g0326 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.415-956A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170150200 | ||||||
| chr3:170150201
|
T | C | 1 | a0001c0001t0025g0292 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.415-957A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170150201 | ||||||
| chr3:170150231
|
C | T | 120 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(117): Show | 121 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.415-987G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170150231 | ||||||
| chr3:170150245
|
A | C | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.415-1001T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170150245 | ||||||
| chr3:170150247
|
G | T | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.415-1003C>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170150247 | ||||||
| chr3:170150471
|
G | A | 4 | a0001c0003t0006g0293a0001c0003t0006g0294a0001c0003t0006g0295others(1): Show | 4 | HG02976.hp2 HG03453.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.415-1227C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170150471 | ||||||
| chr3:170150531
|
T | TA | 12 | a0001c0001t0002g0184a0001c0001t0002g0186a0001c0001t0002g0284others(9): Show | 12 | HG02080.hp1 HG02572.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.415-1288dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170150531 | ||||||
| chr3:170150531
|
T | TAAAAAAA others(3): Show |
66 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(63): Show | 67 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.415-1297_415-1288d others(12): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170150531 | ||||||
| chr3:170150531
|
T | TAAAAAAA others(4): Show |
35 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0026others(32): Show | 35 | HG00597.hp2 HG01109.hp1 HG01123.hp2 others(32): Show |
intron_variant | MODIFIER | c.415-1298_415-1288d others(13): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170150531 | ||||||
| chr3:170150531
|
T | TAAAAAAA others(5): Show |
13 | a0001c0001t0001g0010a0001c0001t0001g0041a0001c0001t0010g0028others(10): Show | 13 | HG00438.hp1 HG01167.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.415-1299_415-1288d others(14): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170150531 | ||||||
| chr3:170150531
|
T | TAAAAAAA others(6): Show |
3 | a0001c0001t0001g0108a0001c0001t0043g0030a0009c0010t0001g0107 | 3 | HG02257.hp1 HG02572.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.415-1300_415-1288d others(15): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170150531 | ||||||
| chr3:170150531
|
TA | T | 19 | a0001c0001t0002g0118a0001c0001t0002g0132a0001c0001t0002g0241others(16): Show | 19 | HG01168.hp1 HG01433.hp1 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.415-1288delT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170150531 | ||||||
| chr3:170150555
|
T | A | 1 | a0004c0012t0004g0173 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.415-1311A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170150555 | ||||||
| chr3:170150555
|
T | C | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.415-1311A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170150555 | ||||||
| chr3:170150557
|
A | T | 1 | a0004c0012t0004g0173 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.415-1313T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170150557 | ||||||
| chr3:170150637
|
T | C | 1 | a0001c0001t0018g0140 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.415-1393A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170150637 | ||||||
| chr3:170150691
|
C | T | 2 | a0001c0003t0006g0294a0001c0003t0006g0295 | 2 | HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.415-1447G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170150691 | ||||||
| chr3:170150719
|
G | A | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.415-1475C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170150719 | ||||||
| chr3:170150817
|
T | C | 1 | a0001c0001t0008g0175 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.415-1573A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170150817 | ||||||
| chr3:170150932
|
G | T | 46 | a0001c0001t0004g0005a0001c0001t0004g0006a0001c0001t0004g0127others(43): Show | 47 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.415-1688C>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170150932 | ||||||
| chr3:170150949
|
C | A | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.415-1705G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170150949 | ||||||
| chr3:170150996
|
A | G | 2 | a0001c0001t0002g0240a0001c0001t0002g0248 | 2 | HG01517.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.415-1752T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170150996 | ||||||
| chr3:170151016
|
G | A | 1 | a0001c0001t0001g0010 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.415-1772C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170151016 | ||||||
| chr3:170151055
|
A | G | 7 | a0001c0001t0003g0257a0001c0001t0003g0258a0001c0001t0003g0259others(4): Show | 7 | HG01255.hp2 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.415-1811T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170151055 | ||||||
| chr3:170151061
|
A | C | 19 | a0001c0002t0005g0305a0001c0002t0005g0306a0001c0002t0005g0307others(16): Show | 19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.415-1817T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170151061 | ||||||
| chr3:170151303
|
T | A | 1 | a0001c0001t0002g0222 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.415-2059A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170151303 | ||||||
| chr3:170151335
|
T | C | 6 | a0001c0001t0012g0100a0001c0001t0012g0102a0001c0001t0012g0103others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.415-2091A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170151335 | ||||||
| chr3:170151368
|
T | C | 2 | a0001c0001t0001g0108a0009c0010t0001g0107 | 2 | HG02257.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.415-2124A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170151368 | ||||||
| chr3:170151384
|
T | C | 1 | a0001c0001t0011g0291 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.415-2140A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170151384 | ||||||
| chr3:170151743
|
G | C | 124 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(121): Show | 125 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.415-2499C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170151743 | ||||||
| chr3:170152337
|
A | AT | 42 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0032others(39): Show | 43 | HG00597.hp1 HG00609.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.415-3094dupA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170152337 | ||||||
| chr3:170152337
|
A | ATT | 6 | a0001c0001t0002g0278a0001c0001t0004g0139a0001c0001t0007g0152others(3): Show | 6 | HG01346.hp1 HG01433.hp1 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.415-3095_415-3094d others(4): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170152337 | ||||||
| chr3:170152337
|
A | T | 3 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0059 | 3 | NA19065.hp1 NA19074.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.415-3093T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170152337 | ||||||
| chr3:170152337
|
AT | A | 26 | a0001c0001t0002g0184a0001c0001t0006g0004a0001c0001t0006g0189others(23): Show | 26 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.415-3094delA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170152337 | ||||||
| chr3:170152385
|
A | C | 1 | a0001c0001t0003g0257 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.415-3141T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170152385 | ||||||
| chr3:170152427
|
C | G | 1 | a0001c0002t0005g0320 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.415-3183G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170152427 | ||||||
| chr3:170152564
|
A | T | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.415-3320T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170152564 | ||||||
| chr3:170152573
|
A | T | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.415-3329T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170152573 | ||||||
| chr3:170152677
|
T | C | 5 | a0001c0001t0003g0188a0001c0001t0003g0233a0001c0001t0003g0267others(2): Show | 5 | HG01081.hp1 HG01361.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.415-3433A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170152677 | ||||||
| chr3:170152861
|
CATGT | C | 3 | a0001c0001t0010g0028a0001c0001t0010g0029a0001c0001t0043g0030 | 3 | HG02615.hp1 HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.415-3621_415-3618d others(6): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170152861 | ||||||
| chr3:170152867
|
G | A | 3 | a0001c0001t0010g0028a0001c0001t0010g0029a0001c0001t0043g0030 | 3 | HG02615.hp1 HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.415-3623C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170152867 | ||||||
| chr3:170152868
|
C | CAA | 3 | a0001c0001t0010g0028a0001c0001t0010g0029a0001c0001t0043g0030 | 3 | HG02615.hp1 HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.415-3625_415-3624i others(4): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170152868 | ||||||
| chr3:170152877
|
G | C | 1 | a0001c0001t0001g0300 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.415-3633C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170152877 | ||||||
| chr3:170153032
|
C | T | 3 | a0001c0001t0008g0175a0001c0001t0008g0176a0001c0001t0008g0177 | 3 | HG02630.hp2 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.415-3788G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170153032 | ||||||
| chr3:170153123
|
T | C | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.415-3879A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170153123 | ||||||
| chr3:170153321
|
T | G | 2 | a0003c0005t0027g0324a0003c0005t0028g0325 | 2 | HG01433.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.415-4077A>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170153321 | ||||||
| chr3:170153356
|
C | T | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.415-4112G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170153356 | ||||||
| chr3:170153444
|
G | A | 1 | a0001c0001t0004g0137 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.415-4200C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170153444 | ||||||
| chr3:170153530
|
G | A | 15 | a0001c0002t0005g0305a0001c0002t0005g0306a0001c0002t0005g0310others(12): Show | 15 | HG00408.hp1 HG00423.hp1 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.415-4286C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170153530 | ||||||
| chr3:170153539
|
G | A | 100 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(97): Show | 101 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.415-4295C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170153539 | ||||||
| chr3:170153595
|
C | G | 31 | a0001c0001t0004g0005a0001c0001t0004g0006a0001c0001t0004g0128others(28): Show | 32 | HG00597.hp1 HG00609.hp2 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.415-4351G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170153595 | ||||||
| chr3:170153622
|
G | A | 1 | a0001c0001t0018g0170 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.415-4378C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170153622 | ||||||
| chr3:170153653
|
C | T | 3 | a0001c0001t0010g0028a0001c0001t0010g0029a0001c0001t0043g0030 | 3 | HG02615.hp1 HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.415-4409G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170153653 | ||||||
| chr3:170153655
|
C | A | 1 | a0001c0001t0002g0218 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.415-4411G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170153655 | ||||||
| chr3:170153672
|
A | G | 1 | a0001c0001t0001g0041 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.415-4428T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170153672 | ||||||
| chr3:170153680
|
G | A | 121 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(118): Show | 122 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.415-4436C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170153680 | ||||||
| chr3:170153719
|
C | T | 1 | a0001c0001t0009g0068 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.415-4475G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170153719 | ||||||
| chr3:170153762
|
C | CA | 107 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(104): Show | 108 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.415-4519dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170153762 | ||||||
| chr3:170153804
|
CT | C | 3 | a0001c0001t0001g0034a0001c0001t0021g0085a0001c0001t0021g0088 | 3 | HG03239.hp1 HG04184.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.415-4561delA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170153804 | ||||||
| chr3:170153839
|
C | A | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.415-4595G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170153839 | ||||||
| chr3:170153914
|
G | A | 1 | a0011c0006t0002g0122 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.415-4670C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170153914 | ||||||
| chr3:170153994
|
C | G | 2 | a0001c0001t0002g0214a0001c0001t0002g0286 | 2 | HG00609.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.415-4750G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170153994 | ||||||
| chr3:170154359
|
C | T | 1 | a0001c0001t0001g0040 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.415-5115G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170154359 | ||||||
| chr3:170154428
|
T | A | 1 | a0001c0001t0003g0200 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.415-5184A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170154428 | ||||||
| chr3:170154459
|
CAGTA | C | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.415-5219_415-5216d others(6): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170154459 | ||||||
| chr3:170154543
|
T | C | 1 | a0001c0001t0046g0277 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.415-5299A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170154543 | ||||||
| chr3:170154560
|
A | T | 1 | a0001c0001t0026g0274 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.415-5316T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170154560 | ||||||
| chr3:170154587
|
T | G | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.415-5343A>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170154587 | ||||||
| chr3:170154638
|
G | T | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.415-5394C>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170154638 | ||||||
| chr3:170154712
|
T | A | 1 | a0001c0001t0001g0031 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.415-5468A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170154712 | ||||||
| chr3:170154811
|
G | T | 2 | a0001c0001t0004g0165a0001c0001t0004g0174 | 2 | HG02486.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.415-5567C>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170154811 | ||||||
| chr3:170154961
|
A | G | 1 | a0001c0001t0053g0178 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.415-5717T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170154961 | ||||||
| chr3:170155013
|
T | C | 3 | a0001c0001t0008g0175a0001c0001t0008g0176a0001c0001t0008g0177 | 3 | HG02630.hp2 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.415-5769A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170155013 | ||||||
| chr3:170155024
|
A | G | 1 | a0001c0001t0003g0228 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.415-5780T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170155024 | ||||||
| chr3:170155046
|
C | T | 49 | a0001c0001t0004g0005a0001c0001t0004g0006a0001c0001t0004g0127others(46): Show | 50 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.415-5802G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170155046 | ||||||
| chr3:170155142
|
A | G | 2 | a0003c0005t0027g0324a0003c0005t0028g0325 | 2 | HG01433.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.415-5898T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170155142 | ||||||
| chr3:170155282
|
A | G | 2 | a0001c0001t0004g0151a0004c0012t0004g0173 | 2 | NA18944.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.415-6038T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170155282 | ||||||
| chr3:170155461
|
C | T | 1 | a0001c0001t0055g0138 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.415-6217G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170155461 | ||||||
| chr3:170155501
|
G | A | 2 | a0003c0005t0027g0324a0003c0005t0028g0325 | 2 | HG01433.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.415-6257C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170155501 | ||||||
| chr3:170155618
|
C | A | 191 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(188): Show | 193 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.415-6374G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170155618 | ||||||
| chr3:170155631
|
A | AG | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.415-6388dupC | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170155631 | ||||||
| chr3:170155682
|
C | A | 1 | a0011c0006t0002g0122 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.415-6438G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170155682 | ||||||
| chr3:170156201
|
T | C | 2 | a0001c0001t0001g0108a0009c0010t0001g0107 | 2 | HG02257.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.415-6957A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170156201 | ||||||
| chr3:170156441
|
G | A | 1 | a0001c0001t0001g0043 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.415-7197C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170156441 | ||||||
| chr3:170156504
|
G | A | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.415-7260C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170156504 | ||||||
| chr3:170156609
|
T | G | 1 | a0005c0011t0002g0237 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.415-7365A>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170156609 | ||||||
| chr3:170156717
|
C | A | 2 | a0001c0001t0010g0028a0001c0001t0010g0029 | 2 | HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.415-7473G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170156717 | ||||||
| chr3:170156846
|
C | T | 41 | a0001c0001t0004g0005a0001c0001t0004g0006a0001c0001t0004g0127others(38): Show | 42 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.415-7602G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170156846 | ||||||
| chr3:170156859
|
T | C | 1 | a0001c0001t0001g0015 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.415-7615A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170156859 | ||||||
| chr3:170156884
|
C | T | 1 | a0001c0001t0041g0207 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.415-7640G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170156884 | ||||||
| chr3:170157028
|
A | G | 1 | a0001c0001t0002g0180 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.415-7784T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170157028 | ||||||
| chr3:170157180
|
T | C | 42 | a0001c0001t0004g0005a0001c0001t0004g0006a0001c0001t0004g0127others(39): Show | 43 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.415-7936A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170157180 | ||||||
| chr3:170157378
|
T | A | 1 | a0001c0001t0056g0160 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.415-8134A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170157378 | ||||||
| chr3:170157457
|
G | A | 1 | a0001c0001t0004g0167 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.415-8213C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170157457 | ||||||
| chr3:170157578
|
A | T | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.415-8334T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170157578 | ||||||
| chr3:170157601
|
A | T | 1 | a0001c0001t0001g0040 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.415-8357T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170157601 | ||||||
| chr3:170157927
|
C | T | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.415-8683G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170157927 | ||||||
| chr3:170157942
|
C | T | 1 | a0001c0001t0001g0033 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.415-8698G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170157942 | ||||||
| chr3:170158150
|
G | A | 7 | a0001c0001t0006g0004a0001c0001t0006g0141a0001c0001t0006g0189others(4): Show | 7 | HG01884.hp1 HG02109.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.415-8906C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170158150 | ||||||
| chr3:170158202
|
A | G | 1 | a0001c0001t0037g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.415-8958T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170158202 | ||||||
| chr3:170158203
|
T | G | 1 | a0001c0001t0042g0194 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.415-8959A>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170158203 | ||||||
| chr3:170158480
|
T | C | 4 | a0001c0001t0002g0270a0001c0001t0002g0271a0001c0001t0002g0272others(1): Show | 4 | NA18747.hp1 NA18942.hp1 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.415-9236A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170158480 | ||||||
| chr3:170158499
|
G | A | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.415-9255C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170158499 | ||||||
| chr3:170158560
|
A | G | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.415-9316T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170158560 | ||||||
| chr3:170158626
|
G | GA | 19 | a0001c0002t0005g0305a0001c0002t0005g0306a0001c0002t0005g0307others(16): Show | 19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.415-9383dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170158626 | ||||||
| chr3:170158666
|
C | T | 3 | a0001c0001t0008g0175a0001c0001t0008g0176a0001c0001t0008g0177 | 3 | HG02630.hp2 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.415-9422G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170158666 | ||||||
| chr3:170158673
|
C | T | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.415-9429G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170158673 | ||||||
| chr3:170158708
|
C | G | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.415-9464G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170158708 | ||||||
| chr3:170158927
|
G | GA | 32 | a0001c0001t0004g0135a0001c0001t0004g0136a0001c0001t0004g0144others(29): Show | 32 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.415-9684dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170158927 | ||||||
| chr3:170158970
|
G | A | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.415-9726C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170158970 | ||||||
| chr3:170158977
|
C | T | 46 | a0001c0001t0004g0005a0001c0001t0004g0006a0001c0001t0004g0127others(43): Show | 47 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.415-9733G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170158977 | ||||||
| chr3:170159129
|
C | A | 2 | a0001c0001t0001g0077a0001c0001t0001g0078 | 2 | HG00280.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.415-9885G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170159129 | ||||||
| chr3:170159164
|
CG | C | 6 | a0001c0001t0008g0175a0001c0001t0008g0176a0001c0001t0008g0177others(3): Show | 6 | HG01433.hp1 HG02055.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.415-9921delC | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170159164 | ||||||
| chr3:170159168
|
C | A | 2 | a0001c0003t0006g0294a0001c0003t0006g0295 | 2 | HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.415-9924G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170159168 | ||||||
| chr3:170159251
|
C | CA | 26 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0018others(23): Show | 26 | HG00408.hp2 HG00735.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.415-10008dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170159251 | ||||||
| chr3:170159251
|
CA | C | 74 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0001g0097others(71): Show | 75 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.415-10008delT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170159251 | ||||||
| chr3:170159251
|
CAAAAA | C | 6 | a0001c0001t0008g0175a0001c0001t0008g0176a0001c0001t0008g0177others(3): Show | 6 | HG01433.hp1 HG02055.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.415-10012_415-1000 others(9): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170159251 | ||||||
| chr3:170159251
|
CAAAAAAA others(5): Show |
C | 6 | a0001c0001t0012g0100a0001c0001t0012g0102a0001c0001t0012g0103others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.415-10019_415-1000 others(16): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170159251 | ||||||
| chr3:170159274
|
A | T | 3 | a0002c0004t0017g0062a0002c0004t0017g0063a0002c0004t0017g0196 | 3 | HG02615.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.415-10030T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170159274 | ||||||
| chr3:170159542
|
G | C | 1 | a0001c0001t0042g0194 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.415-10298C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170159542 | ||||||
| chr3:170159653
|
A | C | 1 | a0001c0001t0011g0065 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.415-10409T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170159653 | ||||||
| chr3:170159666
|
C | T | 1 | a0001c0001t0003g0134 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.415-10422G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170159666 | ||||||
| chr3:170159672
|
A | G | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.415-10428T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170159672 | ||||||
| chr3:170159695
|
C | T | 1 | a0001c0001t0011g0065 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.415-10451G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170159695 | ||||||
| chr3:170159710
|
A | T | 1 | a0001c0001t0011g0065 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.415-10466T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170159710 | ||||||
| chr3:170159751
|
C | T | 1 | a0001c0001t0011g0065 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.415-10507G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170159751 | ||||||
| chr3:170159752
|
A | C | 1 | a0001c0001t0011g0065 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.415-10508T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170159752 | ||||||
| chr3:170159753
|
G | T | 1 | a0001c0001t0011g0065 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.415-10509C>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170159753 | ||||||
| chr3:170159773
|
G | GGGTGGGG others(3): Show |
1 | a0001c0001t0011g0065 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.415-10530_415-1052 others(14): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170159773 | ||||||
| chr3:170159775
|
A | G | 1 | a0001c0001t0011g0065 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.415-10531T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170159775 | ||||||
| chr3:170159780
|
A | T | 1 | a0001c0001t0011g0065 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.415-10536T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170159780 | ||||||
| chr3:170159794
|
C | A | 1 | a0001c0001t0011g0065 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.415-10550G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170159794 | ||||||
| chr3:170159831
|
T | C | 1 | a0001c0001t0003g0202 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.415-10587A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170159831 | ||||||
| chr3:170159974
|
C | T | 1 | a0010c0007t0029g0323 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.415-10730G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170159974 | ||||||
| chr3:170160039
|
G | A | 101 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(98): Show | 102 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.415-10795C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170160039 | ||||||
| chr3:170160057
|
A | G | 1 | a0001c0001t0003g0283 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.415-10813T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170160057 | ||||||
| chr3:170160126
|
T | C | 7 | a0001c0001t0006g0004a0001c0001t0006g0141a0001c0001t0006g0189others(4): Show | 7 | HG01884.hp1 HG02109.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.415-10882A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170160126 | ||||||
| chr3:170160200
|
T | C | 1 | a0001c0002t0044g0316 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.415-10956A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170160200 | ||||||
| chr3:170160232
|
T | G | 5 | a0001c0001t0002g0240a0001c0001t0002g0241a0001c0001t0002g0242others(2): Show | 5 | HG00741.hp1 HG01517.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.415-10988A>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170160232 | ||||||
| chr3:170160934
|
A | G | 1 | a0001c0001t0003g0199 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.414+10439T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170160934 | ||||||
| chr3:170161132
|
C | T | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.414+10241G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170161132 | ||||||
| chr3:170161302
|
C | T | 1 | a0001c0001t0001g0044 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.414+10071G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170161302 | ||||||
| chr3:170161325
|
T | C | 1 | a0001c0001t0003g0201 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.414+10048A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170161325 | ||||||
| chr3:170161375
|
C | T | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.414+9998G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170161375 | ||||||
| chr3:170161415
|
C | T | 2 | a0001c0001t0004g0148a0001c0001t0004g0161 | 2 | NA18942.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.414+9958G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170161415 | ||||||
| chr3:170161527
|
G | C | 1 | a0001c0001t0001g0033 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.414+9846C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170161527 | ||||||
| chr3:170161565
|
G | A | 3 | a0001c0001t0008g0175a0001c0001t0008g0176a0001c0001t0008g0177 | 3 | HG02630.hp2 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.414+9808C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170161565 | ||||||
| chr3:170161570
|
A | G | 199 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(196): Show | 201 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.414+9803T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170161570 | ||||||
| chr3:170161636
|
G | A | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.414+9737C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170161636 | ||||||
| chr3:170161685
|
G | A | 1 | a0001c0001t0004g0168 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.414+9688C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170161685 | ||||||
| chr3:170161866
|
C | T | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.414+9507G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170161866 | ||||||
| chr3:170161907
|
C | T | 46 | a0001c0001t0004g0005a0001c0001t0004g0006a0001c0001t0004g0127others(43): Show | 47 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.414+9466G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170161907 | ||||||
| chr3:170161959
|
A | C | 3 | a0001c0001t0008g0175a0001c0001t0008g0176a0001c0001t0008g0177 | 3 | HG02630.hp2 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.414+9414T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170161959 | ||||||
| chr3:170161974
|
T | C | 1 | a0005c0011t0002g0237 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.414+9399A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170161974 | ||||||
| chr3:170162072
|
T | C | 46 | a0001c0001t0004g0005a0001c0001t0004g0006a0001c0001t0004g0127others(43): Show | 47 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.414+9301A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170162072 | ||||||
| chr3:170162131
|
T | C | 1 | a0001c0002t0005g0322 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.414+9242A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170162131 | ||||||
| chr3:170162296
|
T | C | 199 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(196): Show | 201 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.414+9077A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170162296 | ||||||
| chr3:170162356
|
T | C | 1 | a0001c0001t0052g0243 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.414+9017A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170162356 | ||||||
| chr3:170162500
|
T | C | 9 | a0001c0001t0001g0012a0001c0001t0001g0090a0001c0001t0001g0091others(6): Show | 9 | HG00323.hp1 NA18945.hp2 NA18960.hp1 others(6): Show |
intron_variant | MODIFIER | c.414+8873A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170162500 | ||||||
| chr3:170162645
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.414+8728G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170162645 | ||||||
| chr3:170162721
|
C | G | 1 | a0001c0001t0054g0105 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.414+8652G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170162721 | ||||||
| chr3:170162783
|
T | C | 1 | a0001c0001t0001g0031 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.414+8590A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170162783 | ||||||
| chr3:170162799
|
T | G | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.414+8574A>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170162799 | ||||||
| chr3:170162832
|
C | G | 3 | a0001c0001t0012g0102a0001c0001t0012g0103a0001c0001t0012g0104 | 3 | HG01167.hp1 HG01169.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.414+8541G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170162832 | ||||||
| chr3:170162860
|
G | A | 1 | a0001c0001t0009g0068 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.414+8513C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170162860 | ||||||
| chr3:170162873
|
T | C | 100 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(97): Show | 101 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.414+8500A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170162873 | ||||||
| chr3:170162972
|
T | C | 1 | a0001c0001t0002g0281 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.414+8401A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170162972 | ||||||
| chr3:170162975
|
C | T | 1 | a0001c0001t0042g0194 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.414+8398G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170162975 | ||||||
| chr3:170162984
|
TCTC | T | 100 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(97): Show | 101 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.414+8386_414+8388d others(5): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170162984 | ||||||
| chr3:170163044
|
C | T | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.414+8329G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163044 | ||||||
| chr3:170163045
|
G | A | 1 | a0001c0001t0016g0205 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.414+8328C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163045 | ||||||
| chr3:170163133
|
T | C | 1 | a0002c0004t0017g0196 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.414+8240A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163133 | ||||||
| chr3:170163216
|
C | A | 3 | a0001c0001t0003g0227a0001c0001t0022g0234a0001c0001t0050g0269 | 3 | HG00140.hp1 HG00735.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.414+8157G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163216 | ||||||
| chr3:170163268
|
G | T | 1 | a0001c0001t0002g0185 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.414+8105C>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163268 | ||||||
| chr3:170163461
|
A | AGT | 36 | a0001c0001t0001g0058a0001c0001t0002g0271a0001c0001t0002g0272others(33): Show | 37 | HG00597.hp1 HG00609.hp2 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.414+7910_414+7911d others(4): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163461 | ||||||
| chr3:170163461
|
A | AGTGT | 23 | a0001c0001t0001g0035a0001c0001t0002g0270a0001c0001t0002g0275others(20): Show | 23 | HG00408.hp1 HG00423.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.414+7908_414+7911d others(6): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163461 | ||||||
| chr3:170163461
|
A | AGTGTGT | 6 | a0001c0001t0008g0327a0001c0001t0008g0328a0001c0001t0014g0109others(3): Show | 6 | HG00639.hp1 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.414+7906_414+7911d others(8): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163461 | ||||||
| chr3:170163461
|
AGT | A | 62 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0022others(59): Show | 62 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.414+7910_414+7911d others(4): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163461 | ||||||
| chr3:170163461
|
AGTGT | A | 94 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0077others(91): Show | 94 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.414+7908_414+7911d others(6): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163461 | ||||||
| chr3:170163461
|
AGTGTGT | A | 54 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0017others(51): Show | 57 | HG00323.hp1 HG00438.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.414+7906_414+7911d others(8): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163461 | ||||||
| chr3:170163461
|
AGTGTGTG others(1): Show |
A | 4 | a0001c0001t0001g0074a0001c0001t0004g0165a0001c0001t0004g0174others(1): Show | 4 | HG01884.hp2 HG02486.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.414+7904_414+7911d others(10): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163461 | ||||||
| chr3:170163461
|
AGTGTGTG others(5): Show |
A | 1 | a0001c0001t0043g0030 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.414+7900_414+7911d others(14): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163461 | ||||||
| chr3:170163461
|
AGTGTGTG others(7): Show |
A | 4 | a0001c0001t0010g0028a0001c0001t0010g0029a0001c0001t0018g0140others(1): Show | 4 | HG02717.hp2 HG03098.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.414+7898_414+7911d others(16): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163461 | ||||||
| chr3:170163461
|
AGTGTGTG others(11): Show |
A | 5 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0002g0247others(2): Show | 5 | NA18943.hp2 NA18944.hp2 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.414+7894_414+7911d others(20): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163461 | ||||||
| chr3:170163461
|
AGTGTGTG others(15): Show |
A | 1 | a0001c0002t0005g0310 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.414+7890_414+7911d others(24): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163461 | ||||||
| chr3:170163463
|
T | A | 1 | a0003c0005t0028g0325 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.414+7910A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163463 | ||||||
| chr3:170163514
|
T | C | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.414+7859A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163514 | ||||||
| chr3:170163562
|
C | T | 199 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(196): Show | 201 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.414+7811G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163562 | ||||||
| chr3:170163585
|
G | A | 121 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(118): Show | 122 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.414+7788C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163585 | ||||||
| chr3:170163590
|
C | T | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.414+7783G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163590 | ||||||
| chr3:170163766
|
C | G | 192 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(189): Show | 194 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.414+7607G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163766 | ||||||
| chr3:170163766
|
C | T | 9 | a0001c0001t0003g0202a0001c0001t0003g0204a0001c0001t0006g0004others(6): Show | 9 | HG01884.hp1 HG02080.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.414+7607G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163766 | ||||||
| chr3:170163767
|
G | A | 1 | a0001c0001t0013g0008 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.414+7606C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163767 | ||||||
| chr3:170163861
|
C | CA | 18 | a0001c0001t0002g0121a0001c0001t0002g0185a0001c0001t0002g0192others(15): Show | 18 | HG00621.hp1 HG01346.hp2 HG01517.hp1 others(15): Show |
intron_variant | MODIFIER | c.414+7511dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163861 | ||||||
| chr3:170163861
|
C | CAAA | 16 | a0001c0002t0005g0305a0001c0002t0005g0306a0001c0002t0005g0307others(13): Show | 16 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(13): Show |
intron_variant | MODIFIER | c.414+7509_414+7511d others(5): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163861 | ||||||
| chr3:170163861
|
CA | C | 15 | a0001c0001t0002g0270a0001c0001t0003g0197a0001c0001t0003g0201others(12): Show | 17 | HG00438.hp2 HG00639.hp2 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.414+7511delT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163861 | ||||||
| chr3:170163861
|
CAAAAAAA others(2): Show |
C | 6 | a0001c0001t0012g0100a0001c0001t0012g0102a0001c0001t0012g0103others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.414+7503_414+7511d others(11): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163861 | ||||||
| chr3:170163861
|
CAAAAAAA others(3): Show |
C | 112 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(109): Show | 113 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.414+7502_414+7511d others(12): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163861 | ||||||
| chr3:170163861
|
CAAAAAAA others(4): Show |
C | 3 | a0001c0001t0010g0028a0001c0001t0010g0029a0001c0001t0043g0030 | 3 | HG02615.hp1 HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.414+7501_414+7511d others(13): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163861 | ||||||
| chr3:170163883
|
A | AAAAAAAG others(22): Show |
2 | a0003c0005t0027g0324a0003c0005t0028g0325 | 2 | HG01433.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.414+7489_414+7490i others(31): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163883 | ||||||
| chr3:170163883
|
A | AAAAAGGC others(20): Show |
1 | a0010c0007t0029g0323 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.414+7489_414+7490i others(29): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170163883 | ||||||
| chr3:170164036
|
T | TA | 4 | a0001c0001t0002g0185a0001c0001t0010g0028a0001c0001t0010g0029others(1): Show | 4 | HG02615.hp1 HG02717.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.414+7336dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170164036 | ||||||
| chr3:170164161
|
C | A | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.414+7212G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170164161 | ||||||
| chr3:170164169
|
C | A | 1 | a0001c0001t0003g0266 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.414+7204G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170164169 | ||||||
| chr3:170164222
|
A | C | 1 | a0001c0001t0047g0212 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.414+7151T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170164222 | ||||||
| chr3:170164262
|
A | G | 1 | a0001c0001t0048g0297 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.414+7111T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170164262 | ||||||
| chr3:170164417
|
A | G | 3 | a0001c0001t0008g0175a0001c0001t0008g0176a0001c0001t0008g0177 | 3 | HG02630.hp2 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.414+6956T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170164417 | ||||||
| chr3:170164560
|
G | A | 1 | a0001c0001t0008g0327 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.414+6813C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170164560 | ||||||
| chr3:170164587
|
A | G | 1 | a0001c0001t0002g0223 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.414+6786T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170164587 | ||||||
| chr3:170164830
|
C | A | 19 | a0001c0002t0005g0305a0001c0002t0005g0306a0001c0002t0005g0307others(16): Show | 19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.414+6543G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170164830 | ||||||
| chr3:170165031
|
T | A | 1 | a0001c0001t0002g0275 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.414+6342A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170165031 | ||||||
| chr3:170165041
|
G | A | 1 | a0001c0001t0002g0252 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.414+6332C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170165041 | ||||||
| chr3:170165165
|
T | TC | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.414+6207dupG | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170165165 | ||||||
| chr3:170165208
|
T | C | 6 | a0001c0001t0012g0100a0001c0001t0012g0102a0001c0001t0012g0103others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.414+6165A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170165208 | ||||||
| chr3:170165379
|
G | A | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.414+5994C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170165379 | ||||||
| chr3:170165490
|
T | C | 2 | a0001c0001t0001g0025a0001c0001t0039g0009 | 2 | NA18973.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.414+5883A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170165490 | ||||||
| chr3:170165577
|
A | C | 46 | a0001c0001t0004g0005a0001c0001t0004g0006a0001c0001t0004g0127others(43): Show | 47 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.414+5796T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170165577 | ||||||
| chr3:170165583
|
G | A | 3 | a0001c0001t0001g0018a0001c0001t0001g0027a0001c0001t0001g0120 | 3 | NA18992.hp1 NA19066.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.414+5790C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170165583 | ||||||
| chr3:170165614
|
C | T | 1 | a0001c0001t0018g0140 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.414+5759G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170165614 | ||||||
| chr3:170165742
|
A | T | 1 | a0001c0001t0002g0185 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.414+5631T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170165742 | ||||||
| chr3:170165751
|
C | A | 1 | a0001c0001t0001g0058 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.414+5622G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170165751 | ||||||
| chr3:170165753
|
C | CA | 30 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0034others(27): Show | 30 | HG00423.hp2 HG00544.hp1 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.414+5619dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170165753 | ||||||
| chr3:170165753
|
CA | C | 46 | a0001c0001t0002g0223a0001c0001t0002g0235a0001c0001t0003g0119others(43): Show | 46 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.414+5619delT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170165753 | ||||||
| chr3:170165753
|
CAA | C | 42 | a0001c0001t0004g0005a0001c0001t0004g0006a0001c0001t0004g0127others(39): Show | 43 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.414+5618_414+5619d others(4): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170165753 | ||||||
| chr3:170165815
|
C | CAAAGAAG others(2852): Show |
1 | a0001c0001t0002g0184 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.414+5557_414+5558i others(2861): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170165815 | ||||||
| chr3:170165815
|
C | CAAAGAAG others(3073): Show |
1 | a0001c0001t0002g0250 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.414+5557_414+5558i others(3082): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170165815 | ||||||
| chr3:170165815
|
C | CAAAGAAG others(3342): Show |
1 | a0001c0001t0002g0185 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.414+5557_414+5558i others(3351): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170165815 | ||||||
| chr3:170165815
|
C | CAAAGAAG others(3509): Show |
1 | a0001c0001t0002g0130 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.414+5557_414+5558i others(3518): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170165815 | ||||||
| chr3:170165981
|
T | TA | 7 | a0001c0001t0001g0290a0001c0001t0002g0186a0001c0001t0002g0223others(4): Show | 7 | HG01255.hp2 HG02056.hp2 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.414+5391dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170165981 | ||||||
| chr3:170165981
|
T | TAA | 19 | a0001c0002t0005g0305a0001c0002t0005g0306a0001c0002t0005g0307others(16): Show | 19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.414+5390_414+5391d others(4): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170165981 | ||||||
| chr3:170165999
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.414+5374G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170165999 | ||||||
| chr3:170166102
|
T | C | 1 | a0001c0001t0010g0096 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.414+5271A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170166102 | ||||||
| chr3:170166179
|
G | A | 19 | a0001c0002t0005g0305a0001c0002t0005g0306a0001c0002t0005g0307others(16): Show | 19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.414+5194C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170166179 | ||||||
| chr3:170166375
|
A | T | 1 | a0001c0001t0007g0143 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.414+4998T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170166375 | ||||||
| chr3:170166470
|
T | C | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.414+4903A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170166470 | ||||||
| chr3:170166675
|
C | CT | 67 | a0001c0001t0002g0118a0001c0001t0002g0121a0001c0001t0002g0123others(64): Show | 67 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.414+4697dupA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170166675 | ||||||
| chr3:170166692
|
C | T | 1 | a0001c0001t0034g0089 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.414+4681G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170166692 | ||||||
| chr3:170166826
|
G | A | 6 | a0001c0001t0012g0100a0001c0001t0012g0102a0001c0001t0012g0103others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.414+4547C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170166826 | ||||||
| chr3:170166940
|
C | A | 1 | a0001c0001t0002g0224 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.414+4433G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170166940 | ||||||
| chr3:170167293
|
C | A | 1 | a0001c0001t0001g0058 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.414+4080G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170167293 | ||||||
| chr3:170167315
|
A | G | 52 | a0001c0001t0004g0005a0001c0001t0004g0006a0001c0001t0004g0127others(49): Show | 53 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.414+4058T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170167315 | ||||||
| chr3:170167429
|
T | A | 1 | a0001c0001t0001g0086 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.414+3944A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170167429 | ||||||
| chr3:170167738
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.414+3635G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170167738 | ||||||
| chr3:170167750
|
G | T | 118 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(115): Show | 119 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.414+3623C>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170167750 | ||||||
| chr3:170167759
|
C | CA | 162 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(159): Show | 164 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.414+3613dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170167759 | ||||||
| chr3:170167759
|
C | CAA | 12 | a0001c0001t0001g0034a0001c0001t0008g0113a0001c0001t0008g0116others(9): Show | 12 | HG00438.hp1 HG00597.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.414+3612_414+3613d others(4): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170167759 | ||||||
| chr3:170167759
|
CA | C | 19 | a0001c0001t0002g0229a0001c0001t0003g0188a0001c0001t0003g0201others(16): Show | 19 | HG00140.hp1 HG00735.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.414+3613delT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170167759 | ||||||
| chr3:170167795
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.414+3578G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170167795 | ||||||
| chr3:170167912
|
C | T | 3 | a0001c0001t0008g0175a0001c0001t0008g0176a0001c0001t0008g0177 | 3 | HG02630.hp2 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.414+3461G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170167912 | ||||||
| chr3:170168034
|
C | T | 1 | a0001c0001t0007g0143 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.414+3339G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170168034 | ||||||
| chr3:170168172
|
T | C | 1 | a0001c0001t0047g0212 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.414+3201A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170168172 | ||||||
| chr3:170168185
|
T | TCAAAGG | 198 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(195): Show | 200 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.414+3182_414+3187d others(8): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170168185 | ||||||
| chr3:170168186
|
C | CAAAGGCA others(5): Show |
1 | a0001c0002t0005g0305 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.414+3186_414+3187i others(14): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170168186 | ||||||
| chr3:170168204
|
A | G | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.414+3169T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170168204 | ||||||
| chr3:170168219
|
CCT | C | 6 | a0001c0001t0012g0100a0001c0001t0012g0102a0001c0001t0012g0103others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.414+3152_414+3153d others(4): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170168219 | ||||||
| chr3:170168234
|
G | GA | 10 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0090others(7): Show | 10 | HG00323.hp1 NA18945.hp2 NA18960.hp1 others(7): Show |
intron_variant | MODIFIER | c.414+3138dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170168234 | ||||||
| chr3:170168484
|
G | A | 6 | a0001c0001t0012g0100a0001c0001t0012g0102a0001c0001t0012g0103others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.414+2889C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170168484 | ||||||
| chr3:170168540
|
T | C | 325 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(322): Show | 329 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.414+2833A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170168540 | ||||||
| chr3:170168544
|
T | A | 1 | a0001c0001t0002g0224 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.414+2829A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170168544 | ||||||
| chr3:170168626
|
C | T | 5 | a0001c0001t0001g0011a0001c0001t0001g0036a0001c0001t0001g0037others(2): Show | 5 | HG01256.hp2 HG01515.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.414+2747G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170168626 | ||||||
| chr3:170168703
|
G | A | 1 | a0001c0001t0008g0177 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.414+2670C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170168703 | ||||||
| chr3:170168707
|
T | C | 1 | a0001c0001t0002g0132 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.414+2666A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170168707 | ||||||
| chr3:170168710
|
C | A | 1 | a0001c0001t0003g0267 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.414+2663G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170168710 | ||||||
| chr3:170168753
|
C | CA | 169 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(166): Show | 171 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.414+2619dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170168753 | ||||||
| chr3:170168753
|
C | CAA | 22 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0026others(19): Show | 22 | HG00438.hp1 HG00597.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.414+2618_414+2619d others(4): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170168753 | ||||||
| chr3:170168753
|
C | CAAA | 14 | a0001c0002t0005g0305a0001c0002t0005g0306a0001c0002t0005g0307others(11): Show | 14 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(11): Show |
intron_variant | MODIFIER | c.414+2617_414+2619d others(5): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170168753 | ||||||
| chr3:170168820
|
T | A | 2 | a0001c0001t0001g0018a0001c0001t0001g0027 | 2 | NA19066.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.414+2553A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170168820 | ||||||
| chr3:170168900
|
A | G | 1 | a0001c0001t0003g0197 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.414+2473T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170168900 | ||||||
| chr3:170168938
|
G | T | 3 | a0001c0001t0008g0113a0001c0001t0008g0116a0001c0001t0008g0117 | 3 | HG02622.hp2 HG02818.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.414+2435C>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170168938 | ||||||
| chr3:170169041
|
C | T | 21 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0129others(18): Show | 21 | HG00140.hp2 HG00280.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.414+2332G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170169041 | ||||||
| chr3:170169068
|
G | A | 4 | a0001c0001t0003g0179a0001c0001t0003g0209a0001c0001t0003g0210others(1): Show | 4 | HG02145.hp1 HG02970.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.414+2305C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170169068 | ||||||
| chr3:170169095
|
C | T | 2 | a0001c0001t0002g0214a0001c0001t0002g0286 | 2 | HG00609.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.414+2278G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170169095 | ||||||
| chr3:170169282
|
C | T | 2 | a0003c0005t0027g0324a0003c0005t0028g0325 | 2 | HG01433.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.414+2091G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170169282 | ||||||
| chr3:170169299
|
T | C | 1 | a0001c0002t0005g0308 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.414+2074A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170169299 | ||||||
| chr3:170169326
|
A | G | 121 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(118): Show | 122 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.414+2047T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170169326 | ||||||
| chr3:170169614
|
T | C | 1 | a0001c0001t0042g0194 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.414+1759A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170169614 | ||||||
| chr3:170170043
|
C | A | 46 | a0001c0001t0004g0005a0001c0001t0004g0006a0001c0001t0004g0127others(43): Show | 47 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.414+1330G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170170043 | ||||||
| chr3:170170150
|
C | G | 2 | a0001c0001t0010g0028a0001c0001t0010g0029 | 2 | HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.414+1223G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170170150 | ||||||
| chr3:170170472
|
G | A | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.414+901C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170170472 | ||||||
| chr3:170170704
|
T | C | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.414+669A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170170704 | ||||||
| chr3:170171159
|
A | T | 1 | a0001c0002t0044g0316 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.414+214T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170171159 | ||||||
| chr3:170171187
|
C | CA | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.414+185dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170171187 | ||||||
| chr3:170171258
|
C | G | 1 | a0001c0001t0001g0074 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.414+115G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170171258 | ||||||
| chr3:170171276
|
A | C | 2 | a0001c0003t0006g0294a0001c0003t0006g0295 | 2 | HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.414+97T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 4/14 | chr3 | 170171276 | ||||||
| chr3:170171543
|
T | A | 46 | a0001c0001t0004g0005a0001c0001t0004g0006a0001c0001t0004g0127others(43): Show | 47 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.337-93A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 3/14 | chr3 | 170171543 | ||||||
| chr3:170171917
|
G | C | 1 | a0001c0001t0046g0277 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.337-467C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 3/14 | chr3 | 170171917 | ||||||
| chr3:170171976
|
C | A | 121 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(118): Show | 122 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.337-526G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 3/14 | chr3 | 170171976 | ||||||
| chr3:170172115
|
C | T | 121 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(118): Show | 122 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.336+442G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 3/14 | chr3 | 170172115 | ||||||
| chr3:170172374
|
T | TA | 121 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(118): Show | 122 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.336+182dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 3/14 | chr3 | 170172374 | ||||||
| chr3:170172397
|
T | A | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.336+160A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 3/14 | chr3 | 170172397 | ||||||
| chr3:170172487
|
C | G | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.336+70G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 3/14 | chr3 | 170172487 | ||||||
| chr3:170172545
|
T | C | 1 | a0001c0001t0010g0020 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.336+12A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 3/14 | chr3 | 170172545 | ||||||
| chr3:170172799
|
T | C | 5 | a0001c0001t0012g0100a0001c0001t0012g0102a0001c0001t0012g0103others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.181-87A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170172799 | ||||||
| chr3:170172864
|
A | G | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.181-152T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170172864 | ||||||
| chr3:170172934
|
GT | G | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.181-223delA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170172934 | ||||||
| chr3:170172950
|
T | C | 46 | a0001c0001t0004g0005a0001c0001t0004g0006a0001c0001t0004g0127others(43): Show | 47 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.181-238A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170172950 | ||||||
| chr3:170172966
|
G | A | 1 | a0001c0001t0002g0278 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.181-254C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170172966 | ||||||
| chr3:170173016
|
C | A | 1 | a0001c0001t0042g0194 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.181-304G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170173016 | ||||||
| chr3:170173019
|
C | T | 1 | a0001c0001t0002g0192 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.181-307G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170173019 | ||||||
| chr3:170173134
|
G | A | 1 | a0001c0001t0037g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.181-422C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170173134 | ||||||
| chr3:170173172
|
G | A | 4 | a0001c0001t0001g0066a0003c0005t0027g0324a0003c0005t0028g0325others(1): Show | 4 | HG01433.hp1 HG02055.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.181-460C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170173172 | ||||||
| chr3:170173202
|
A | C | 1 | a0001c0001t0043g0030 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.181-490T>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170173202 | ||||||
| chr3:170173206
|
A | G | 1 | a0001c0001t0010g0020 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.181-494T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170173206 | ||||||
| chr3:170173245
|
C | G | 1 | a0001c0013t0002g0213 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.181-533G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170173245 | ||||||
| chr3:170173284
|
A | G | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.181-572T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170173284 | ||||||
| chr3:170173391
|
T | C | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.181-679A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170173391 | ||||||
| chr3:170173397
|
G | A | 2 | a0001c0001t0006g0279a0001c0001t0006g0280 | 2 | HG01884.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.181-685C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170173397 | ||||||
| chr3:170173414
|
C | T | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.181-702G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170173414 | ||||||
| chr3:170173451
|
C | G | 3 | a0001c0001t0008g0175a0001c0001t0008g0176a0001c0001t0008g0177 | 3 | HG02630.hp2 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.181-739G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170173451 | ||||||
| chr3:170173458
|
G | A | 49 | a0001c0001t0004g0005a0001c0001t0004g0006a0001c0001t0004g0127others(46): Show | 50 | HG00597.hp1 HG00609.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.181-746C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170173458 | ||||||
| chr3:170173673
|
T | C | 19 | a0001c0002t0005g0305a0001c0002t0005g0306a0001c0002t0005g0307others(16): Show | 19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.181-961A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170173673 | ||||||
| chr3:170173844
|
C | T | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.181-1132G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170173844 | ||||||
| chr3:170173854
|
T | C | 1 | a0001c0001t0042g0194 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.181-1142A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170173854 | ||||||
| chr3:170173935
|
G | A | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.181-1223C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170173935 | ||||||
| chr3:170174123
|
G | A | 1 | a0001c0001t0054g0105 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.181-1411C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170174123 | ||||||
| chr3:170174166
|
C | CTCT | 6 | a0001c0001t0012g0100a0001c0001t0012g0102a0001c0001t0012g0103others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.181-1455_181-1454i others(5): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170174166 | ||||||
| chr3:170174277
|
A | T | 7 | a0001c0001t0008g0113a0001c0001t0008g0116a0001c0001t0008g0117others(4): Show | 7 | HG00639.hp1 HG02055.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.181-1565T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170174277 | ||||||
| chr3:170174278
|
A | T | 120 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(117): Show | 121 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.181-1566T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170174278 | ||||||
| chr3:170174439
|
A | G | 3 | a0002c0004t0017g0062a0002c0004t0017g0063a0002c0004t0017g0196 | 3 | HG02615.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.181-1727T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170174439 | ||||||
| chr3:170174510
|
G | A | 191 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(188): Show | 193 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.181-1798C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170174510 | ||||||
| chr3:170174958
|
A | G | 2 | a0001c0002t0005g0306a0001c0002t0005g0319 | 2 | NA18964.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.181-2246T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170174958 | ||||||
| chr3:170175027
|
A | G | 3 | a0001c0001t0014g0109a0001c0001t0014g0110a0001c0001t0014g0111 | 3 | HG02257.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.181-2315T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170175027 | ||||||
| chr3:170175269
|
T | C | 1 | a0001c0001t0002g0281 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.181-2557A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170175269 | ||||||
| chr3:170175394
|
T | G | 1 | a0001c0001t0032g0115 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.181-2682A>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170175394 | ||||||
| chr3:170175610
|
C | G | 191 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(188): Show | 193 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.181-2898G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170175610 | ||||||
| chr3:170175636
|
A | G | 6 | a0001c0001t0012g0100a0001c0001t0012g0102a0001c0001t0012g0103others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.181-2924T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170175636 | ||||||
| chr3:170175637
|
G | A | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.181-2925C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170175637 | ||||||
| chr3:170175747
|
G | A | 306 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(303): Show | 310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.180+3026C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170175747 | ||||||
| chr3:170175760
|
T | C | 1 | a0001c0001t0010g0029 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.180+3013A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170175760 | ||||||
| chr3:170175838
|
C | T | 3 | a0001c0001t0008g0175a0001c0001t0008g0176a0001c0001t0008g0177 | 3 | HG02630.hp2 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.180+2935G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170175838 | ||||||
| chr3:170175902
|
C | T | 1 | a0001c0001t0053g0178 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.180+2871G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170175902 | ||||||
| chr3:170175908
|
G | A | 5 | a0001c0001t0008g0113a0001c0001t0008g0116a0001c0001t0008g0117others(2): Show | 5 | HG02055.hp2 HG02622.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.180+2865C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170175908 | ||||||
| chr3:170175923
|
C | CA | 29 | a0001c0001t0002g0192a0001c0001t0002g0284a0001c0001t0002g0285others(26): Show | 29 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.180+2849dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170175923 | ||||||
| chr3:170175938
|
C | A | 1 | a0003c0005t0028g0325 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.180+2835G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170175938 | ||||||
| chr3:170175966
|
G | A | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.180+2807C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170175966 | ||||||
| chr3:170176205
|
G | A | 2 | a0001c0002t0005g0315a0008c0014t0005g0321 | 2 | HG02027.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.180+2568C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170176205 | ||||||
| chr3:170176218
|
T | C | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.180+2555A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170176218 | ||||||
| chr3:170176225
|
C | CA | 121 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(118): Show | 122 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.180+2547dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170176225 | ||||||
| chr3:170176245
|
AG | A | 3 | a0001c0001t0002g0289a0001c0001t0003g0287a0001c0001t0049g0288 | 3 | NA18959.hp1 NA18986.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.180+2527delC | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170176245 | ||||||
| chr3:170176421
|
A | G | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.180+2352T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170176421 | ||||||
| chr3:170176437
|
G | C | 1 | a0010c0007t0029g0323 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.180+2336C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170176437 | ||||||
| chr3:170176440
|
G | A | 1 | a0001c0002t0005g0317 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.180+2333C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170176440 | ||||||
| chr3:170176452
|
T | C | 1 | a0001c0001t0037g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.180+2321A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170176452 | ||||||
| chr3:170176509
|
G | A | 1 | a0011c0006t0002g0122 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.180+2264C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170176509 | ||||||
| chr3:170176552
|
G | A | 1 | a0001c0001t0006g0141 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.180+2221C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170176552 | ||||||
| chr3:170176555
|
C | G | 189 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(186): Show | 191 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.180+2218G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170176555 | ||||||
| chr3:170176726
|
G | A | 5 | a0001c0001t0012g0100a0001c0001t0012g0102a0001c0001t0012g0103others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.180+2047C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170176726 | ||||||
| chr3:170176892
|
G | A | 189 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(186): Show | 191 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.180+1881C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170176892 | ||||||
| chr3:170176918
|
T | C | 3 | a0001c0001t0012g0102a0001c0001t0012g0103a0001c0001t0012g0104 | 3 | HG01167.hp1 HG01169.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.180+1855A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170176918 | ||||||
| chr3:170176929
|
A | T | 1 | a0007c0009t0001g0019 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.180+1844T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170176929 | ||||||
| chr3:170176954
|
A | G | 1 | a0001c0001t0007g0142 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.180+1819T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170176954 | ||||||
| chr3:170177022
|
A | G | 1 | a0001c0001t0042g0194 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.180+1751T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170177022 | ||||||
| chr3:170177203
|
A | G | 8 | a0001c0001t0009g0002a0001c0001t0009g0064a0001c0001t0009g0067others(5): Show | 9 | HG01109.hp1 HG01257.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.180+1570T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170177203 | ||||||
| chr3:170177214
|
T | G | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.180+1559A>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170177214 | ||||||
| chr3:170177230
|
G | C | 189 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(186): Show | 191 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.180+1543C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170177230 | ||||||
| chr3:170177236
|
A | G | 192 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(189): Show | 194 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.180+1537T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170177236 | ||||||
| chr3:170177417
|
A | T | 2 | a0001c0003t0006g0294a0001c0003t0006g0295 | 2 | HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.180+1356T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170177417 | ||||||
| chr3:170177428
|
G | A | 1 | a0001c0001t0013g0008 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.180+1345C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170177428 | ||||||
| chr3:170177489
|
C | T | 1 | a0001c0001t0002g0193 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.180+1284G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170177489 | ||||||
| chr3:170177609
|
C | T | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.180+1164G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170177609 | ||||||
| chr3:170177658
|
C | T | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.180+1115G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170177658 | ||||||
| chr3:170177666
|
A | AT | 159 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(156): Show | 161 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.180+1106dupA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170177666 | ||||||
| chr3:170177666
|
A | ATT | 43 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0016others(40): Show | 43 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.180+1105_180+1106d others(4): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170177666 | ||||||
| chr3:170177696
|
G | C | 1 | a0001c0001t0003g0134 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.180+1077C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170177696 | ||||||
| chr3:170177859
|
T | TG | 113 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(110): Show | 114 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.180+913dupC | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170177859 | ||||||
| chr3:170178140
|
A | AT | 12 | a0001c0001t0001g0010a0001c0001t0002g0129a0001c0001t0002g0130others(9): Show | 12 | HG01175.hp2 HG02080.hp2 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.180+632dupA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170178140 | ||||||
| chr3:170178143
|
T | A | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.180+630A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170178143 | ||||||
| chr3:170178144
|
T | A | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.180+629A>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170178144 | ||||||
| chr3:170178185
|
T | C | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.180+588A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170178185 | ||||||
| chr3:170178210
|
C | G | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.180+563G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170178210 | ||||||
| chr3:170178221
|
G | A | 3 | a0001c0001t0010g0028a0001c0001t0010g0029a0001c0001t0043g0030 | 3 | HG02615.hp1 HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.180+552C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170178221 | ||||||
| chr3:170178235
|
C | G | 42 | a0001c0001t0001g0011a0001c0001t0001g0031a0001c0001t0001g0032others(39): Show | 42 | HG00323.hp2 HG00408.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.180+538G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170178235 | ||||||
| chr3:170178266
|
C | A | 2 | a0001c0001t0001g0108a0009c0010t0001g0107 | 2 | HG02257.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.180+507G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170178266 | ||||||
| chr3:170178366
|
C | T | 1 | a0001c0001t0001g0010 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.180+407G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170178366 | ||||||
| chr3:170178572
|
A | T | 2 | a0001c0001t0002g0123a0001c0001t0002g0124 | 2 | HG00280.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.180+201T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170178572 | ||||||
| chr3:170178709
|
A | G | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.180+64T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 2/14 | chr3 | 170178709 | ||||||
| chr3:170179161
|
T | G | 1 | a0008c0014t0005g0321 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.15-223A>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170179161 | ||||||
| chr3:170179372
|
C | A | 3 | a0001c0001t0014g0109a0001c0001t0014g0110a0001c0001t0014g0111 | 3 | HG02257.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.15-434G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170179372 | ||||||
| chr3:170180133
|
T | TA | 5 | a0001c0001t0043g0030a0001c0002t0005g0322a0003c0005t0027g0324others(2): Show | 5 | HG01433.hp1 HG02055.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.15-1196dupT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170180133 | ||||||
| chr3:170180148
|
CA | C | 23 | a0001c0001t0002g0121a0001c0001t0010g0028a0001c0001t0010g0029others(20): Show | 23 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(20): Show |
intron_variant | MODIFIER | c.15-1211delT | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170180148 | ||||||
| chr3:170180217
|
G | C | 1 | a0001c0001t0025g0292 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.15-1279C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170180217 | ||||||
| chr3:170180263
|
T | G | 1 | a0001c0001t0001g0112 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.15-1325A>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170180263 | ||||||
| chr3:170180305
|
C | T | 1 | a0001c0003t0006g0293 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.15-1367G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170180305 | ||||||
| chr3:170180316
|
G | T | 15 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(12): Show | 15 | HG00544.hp2 HG00558.hp2 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.15-1378C>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170180316 | ||||||
| chr3:170180404
|
G | A | 7 | a0001c0001t0008g0113a0001c0001t0008g0116a0001c0001t0008g0117others(4): Show | 7 | HG00639.hp1 HG02055.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.14+1298C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170180404 | ||||||
| chr3:170180469
|
A | G | 2 | a0001c0001t0002g0118a0001c0001t0003g0119 | 2 | NA18959.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.14+1233T>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170180469 | ||||||
| chr3:170180564
|
G | GT | 112 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(109): Show | 113 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.14+1137dupA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170180564 | ||||||
| chr3:170180564
|
G | GTT | 6 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(3): Show | 6 | HG00741.hp2 HG01123.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.14+1136_14+1137dup others(2): Show |
PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170180564 | ||||||
| chr3:170180564
|
GT | G | 6 | a0001c0001t0003g0298a0001c0001t0048g0297a0001c0003t0006g0293others(3): Show | 6 | HG02976.hp2 HG03453.hp2 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.14+1137delA | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170180564 | ||||||
| chr3:170180631
|
T | C | 4 | a0001c0001t0001g0299a0001c0001t0001g0300a0001c0001t0001g0301others(1): Show | 4 | HG01261.hp2 HG01934.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.14+1071A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170180631 | ||||||
| chr3:170181184
|
T | C | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.14+518A>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170181184 | ||||||
| chr3:170181196
|
G | T | 1 | a0001c0001t0013g0008 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.14+506C>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170181196 | ||||||
| chr3:170181197
|
A | T | 1 | a0001c0001t0013g0008 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.14+505T>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170181197 | ||||||
| chr3:170181406
|
C | A | 1 | a0001c0001t0001g0303 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.14+296G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170181406 | ||||||
| chr3:170181407
|
G | A | 1 | a0001c0001t0035g0304 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.14+295C>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170181407 | ||||||
| chr3:170181432
|
G | C | 19 | a0001c0002t0005g0305a0001c0002t0005g0306a0001c0002t0005g0307others(16): Show | 19 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.14+270C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170181432 | ||||||
| chr3:170181466
|
C | A | 3 | a0003c0005t0027g0324a0003c0005t0028g0325a0010c0007t0029g0323 | 3 | HG01433.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.14+236G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170181466 | ||||||
| chr3:170181484
|
G | C | 2 | a0003c0005t0027g0324a0003c0005t0028g0325 | 2 | HG01433.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.14+218C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170181484 | ||||||
| chr3:170181490
|
G | C | 1 | a0001c0002t0005g0326 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.14+212C>G | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170181490 | ||||||
| chr3:170181514
|
C | T | 1 | a0001c0001t0022g0007 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.14+188G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170181514 | ||||||
| chr3:170181521
|
C | G | 2 | a0001c0001t0004g0005a0001c0001t0004g0006 | 2 | HG00597.hp1 HG00609.hp2 |
intron_variant | MODIFIER | c.14+181G>C | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170181521 | ||||||
| chr3:170181535
|
C | T | 1 | a0001c0001t0006g0004 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.14+167G>A | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170181535 | ||||||
| chr3:170181665
|
C | A | 2 | a0001c0001t0008g0327a0001c0001t0008g0328 | 2 | HG02055.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.14+37G>T | PHC3 | ENSG00000173889.16 | transcript | ENST00000495893.7 | protein_coding | 1/14 | chr3 | 170181665 |