Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 84333 |
| ensemblid | ENSG00000180628.15 |
| hgncid | 28264 |
| symbol | PCGF5 |
| name | polycomb group ring finger 5 |
| refseq_nuc | NM_032373.5 |
| refseq_prot | NP_115749.2 |
| ensembl_nuc | ENST00000336126.6 |
| ensembl_prot | ENSP00000337500.5 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 91220663 |
| end | 91284337 |
| strand | + |
| ver | v1.2 |
| region | chr10:91220663-91284337 |
| region5000 | chr10:91215663-91289337 |
| regionname0 | PCGF5_chr10_91220663_91284337 |
| regionname5000 | PCGF5_chr10_91215663_91289337 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 768 | 316 | 88 | 66 | 122 | 16 | 22 | PCGF5_chr10_91215663_91289337 | PCGF5 | ATGGC others(763): Show |
chr10 | 91215663 | 91289337 | ||
| a0001c0002 | 0/0 | 768 | 2 | 2 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | ATGGC others(763): Show |
chr10 | 91215663 | 91289337 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 7149 | 159 | 24 | 30 | 89 | 5 | 9 | PCGF5_chr10_91215663_91289337 | PCGF5 | GTCGG others(7144): Show |
chr10 | 91215663 | 91289337 |
| a0001c0001t0002 | 0/0 | 7149 | 41 | 0 | 12 | 21 | 3 | 5 | PCGF5_chr10_91215663_91289337 | PCGF5 | GTCGG others(7144): Show |
chr10 | 91215663 | 91289337 |
| a0001c0001t0003 | 0/0 | 7149 | 28 | 16 | 6 | 0 | 5 | 1 | PCGF5_chr10_91215663_91289337 | PCGF5 | GTCGG others(7144): Show |
chr10 | 91215663 | 91289337 |
| a0001c0001t0004 | 0/0 | 7149 | 15 | 13 | 2 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | GTCGG others(7144): Show |
chr10 | 91215663 | 91289337 |
| a0001c0001t0005 | 0/0 | 7149 | 6 | 5 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | GTCGG others(7144): Show |
chr10 | 91215663 | 91289337 |
| a0001c0001t0006 | 0/0 | 7149 | 6 | 5 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | GTCGG others(7144): Show |
chr10 | 91215663 | 91289337 |
| a0001c0001t0007 | 0/0 | 7149 | 5 | 0 | 2 | 0 | 1 | 2 | PCGF5_chr10_91215663_91289337 | PCGF5 | GTCGG others(7144): Show |
chr10 | 91215663 | 91289337 |
| a0001c0001t0008 | 0/0 | 7149 | 5 | 5 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | GTCGG others(7144): Show |
chr10 | 91215663 | 91289337 |
| a0001c0001t0009 | 0/0 | 7149 | 5 | 1 | 4 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | GTCGG others(7144): Show |
chr10 | 91215663 | 91289337 |
| a0001c0001t0010 | 0/0 | 7150 | 4 | 4 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | GTCGG others(7145): Show |
chr10 | 91215663 | 91289337 |
| a0001c0001t0011 | 0/0 | 7149 | 4 | 1 | 1 | 0 | 0 | 2 | PCGF5_chr10_91215663_91289337 | PCGF5 | GTCGG others(7144): Show |
chr10 | 91215663 | 91289337 |
| a0001c0001t0013 | 0/0 | 7149 | 2 | 2 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | GTCGG others(7144): Show |
chr10 | 91215663 | 91289337 |
| a0001c0001t0014 | 0/0 | 7149 | 2 | 2 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | GTCGG others(7144): Show |
chr10 | 91215663 | 91289337 |
| a0001c0001t0015 | 0/0 | 7149 | 2 | 0 | 0 | 0 | 0 | 2 | PCGF5_chr10_91215663_91289337 | PCGF5 | GTCGG others(7144): Show |
chr10 | 91215663 | 91289337 |
| a0001c0001t0016 | 0/0 | 7149 | 2 | 0 | 0 | 2 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | GTCGG others(7144): Show |
chr10 | 91215663 | 91289337 |
| a0001c0001t0017 | 0/0 | 7149 | 2 | 2 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | GTCGG others(7144): Show |
chr10 | 91215663 | 91289337 |
| a0001c0001t0018 | 0/0 | 7149 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | GTCGG others(7144): Show |
chr10 | 91215663 | 91289337 |
| a0001c0001t0019 | 0/0 | 7149 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | GTCGG others(7144): Show |
chr10 | 91215663 | 91289337 |
| a0001c0001t0020 | 0/0 | 7149 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | GTCGG others(7144): Show |
chr10 | 91215663 | 91289337 |
| a0001c0001t0021 | 0/0 | 7149 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | GTCGG others(7144): Show |
chr10 | 91215663 | 91289337 |
| a0001c0001t0022 | 0/0 | 7150 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | GTCGG others(7145): Show |
chr10 | 91215663 | 91289337 |
| a0001c0001t0023 | 0/0 | 7149 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | GTCGG others(7144): Show |
chr10 | 91215663 | 91289337 |
| a0001c0001t0024 | 0/0 | 7149 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | GTCGG others(7144): Show |
chr10 | 91215663 | 91289337 |
| a0001c0001t0025 | 0/0 | 7149 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | GTCGG others(7144): Show |
chr10 | 91215663 | 91289337 |
| a0001c0001t0026 | 0/0 | 7149 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | GTCGG others(7144): Show |
chr10 | 91215663 | 91289337 |
| a0001c0001t0027 | 0/0 | 7149 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | GTCGG others(7144): Show |
chr10 | 91215663 | 91289337 |
| a0001c0001t0028 | 0/0 | 7149 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | GTCGG others(7144): Show |
chr10 | 91215663 | 91289337 |
| a0001c0001t0029 | 0/0 | 7149 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | GTCGG others(7144): Show |
chr10 | 91215663 | 91289337 |
| a0001c0001t0030 | 0/0 | 7149 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | GTCGG others(7144): Show |
chr10 | 91215663 | 91289337 |
| a0001c0001t0031 | 0/0 | 7149 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | GTCGG others(7144): Show |
chr10 | 91215663 | 91289337 |
| a0001c0001t0032 | 0/0 | 7149 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | GTCGG others(7144): Show |
chr10 | 91215663 | 91289337 |
| a0001c0001t0033 | 0/0 | 7150 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | GTCGG others(7145): Show |
chr10 | 91215663 | 91289337 |
| a0001c0001t0034 | 0/0 | 7149 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | GTCGG others(7144): Show |
chr10 | 91215663 | 91289337 |
| a0001c0001t0035 | 0/0 | 7126 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | GTCGG others(7121): Show |
chr10 | 91215663 | 91289337 |
| a0001c0001t0036 | 0/0 | 7149 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | GTCGG others(7144): Show |
chr10 | 91215663 | 91289337 |
| a0001c0001t0037 | 0/0 | 7149 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | GTCGG others(7144): Show |
chr10 | 91215663 | 91289337 |
| a0001c0001t0038 | 0/0 | 7150 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | GTCGG others(7145): Show |
chr10 | 91215663 | 91289337 |
| a0001c0001t0039 | 0/0 | 7149 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | GTCGG others(7144): Show |
chr10 | 91215663 | 91289337 |
| a0001c0001t0040 | 0/0 | 7149 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | GTCGG others(7144): Show |
chr10 | 91215663 | 91289337 |
| a0001c0001t0041 | 0/0 | 7149 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | GTCGG others(7144): Show |
chr10 | 91215663 | 91289337 |
| a0001c0001t0042 | 0/0 | 7149 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | GTCGG others(7144): Show |
chr10 | 91215663 | 91289337 |
| a0001c0001t0043 | 0/0 | 7149 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | GTCGG others(7144): Show |
chr10 | 91215663 | 91289337 |
| a0001c0001t0044 | 0/0 | 7149 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | GTCGG others(7144): Show |
chr10 | 91215663 | 91289337 |
| a0001c0001t0045 | 0/0 | 7149 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF5_chr10_91215663_91289337 | PCGF5 | GTCGG others(7144): Show |
chr10 | 91215663 | 91289337 |
| a0001c0002t0012 | 0/0 | 7149 | 2 | 2 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | GTCGG others(7144): Show |
chr10 | 91215663 | 91289337 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 1 | 2 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0002 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0004 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0005 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0038 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0108 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0002g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0002g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0003g0009 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0003g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0004g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0004g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0004g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0004g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0004g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0005g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0005g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0005g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0005g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0005g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0006g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0006g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0006g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0006g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0006g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0007g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0007g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0007g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0007g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0007g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0008g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0008g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0008g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0008g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0008g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0009g0007 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0009g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0010g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0010g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0010g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0011g0013 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0011g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0013g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0013g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0014g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0014g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0015g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0016g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0016g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0017g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0017g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0018g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0019g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0020g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0021g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0022g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0023g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0024g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0025g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0026g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0027g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0028g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0029g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0030g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0031g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0032g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0033g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0034g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0035g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0036g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0037g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0038g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0039g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0040g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0041g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0042g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0043g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0044g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0001t0045g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| a0001c0002t0012g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0150 | EUR | GBR | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG00099 | hp2 | a0001 | c0001 | t0032 | g0001 | EUR | GBR | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG00140 | hp1 | a0001 | c0001 | t0007 | g0175 | EUR | GBR | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0114 | EUR | GBR | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0009 | EUR | FIN | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0100 | EUR | FIN | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0122 | EUR | FIN | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0075 | EUR | FIN | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | CHS | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | CHS | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | CHS | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0153 | AMR | PUR | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0128 | AMR | PUR | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0161 | AMR | PUR | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG00741 | hp1 | a0001 | c0001 | t0024 | g0009 | AMR | PUR | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0154 | AMR | PUR | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01070 | hp1 | a0001 | c0001 | t0019 | g0235 | AMR | PUR | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0146 | AMR | PUR | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01081 | hp1 | a0001 | c0001 | t0009 | g0007 | AMR | PUR | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01081 | hp2 | a0001 | c0001 | t0006 | g0186 | AMR | PUR | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01106 | hp2 | a0001 | c0001 | t0023 | g0080 | AMR | PUR | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0116 | AMR | PUR | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0141 | AMR | PUR | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0123 | AMR | PUR | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01169 | hp2 | a0001 | c0001 | t0035 | g0016 | AMR | PUR | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0158 | AMR | PUR | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01192 | hp1 | a0001 | c0001 | t0005 | g0192 | AMR | PUR | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01192 | hp2 | a0001 | c0001 | t0009 | g0044 | AMR | PUR | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0026 | AMR | PUR | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0115 | AMR | CLM | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01255 | hp2 | a0001 | c0001 | t0011 | g0013 | AMR | CLM | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01256 | hp1 | a0001 | c0001 | t0041 | g0016 | AMR | CLM | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01256 | hp2 | a0001 | c0001 | t0007 | g0177 | AMR | CLM | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01257 | hp2 | a0001 | c0001 | t0009 | g0007 | AMR | CLM | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01258 | hp1 | a0001 | c0001 | t0009 | g0007 | AMR | CLM | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01258 | hp2 | a0001 | c0001 | t0007 | g0176 | AMR | CLM | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | CLM | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01361 | hp1 | a0001 | c0001 | t0038 | g0001 | AMR | CLM | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | CLM | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0118 | AMR | CLM | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0140 | AMR | CLM | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01515 | hp1 | a0001 | c0001 | t0033 | g0001 | EUR | IBS | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0195 | EUR | IBS | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0024 | EUR | IBS | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0194 | EUR | IBS | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01884 | hp1 | a0001 | c0001 | t0011 | g0101 | AFR | ACB | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01884 | hp2 | a0001 | c0001 | t0017 | g0040 | AFR | ACB | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01891 | hp1 | a0001 | c0001 | t0014 | g0037 | AFR | ACB | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PEL | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01952 | hp1 | a0001 | c0001 | t0029 | g0067 | AMR | PEL | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0142 | AMR | PEL | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0157 | AMR | PEL | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0166 | AFR | ACB | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | KHV | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02135 | hp1 | a0001 | c0001 | t0043 | g0105 | EAS | KHV | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0199 | AFR | ACB | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0041 | AFR | ACB | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PEL | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CDX | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02155 | hp2 | a0001 | c0001 | t0039 | g0237 | EAS | CDX | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0014 | AFR | ACB | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02258 | hp1 | a0001 | c0001 | t0010 | g0196 | AFR | ACB | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0121 | AFR | ACB | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0172 | AFR | ACB | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02280 | hp2 | a0001 | c0001 | t0017 | g0039 | AFR | ACB | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PEL | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02451 | hp2 | a0001 | c0001 | t0008 | g0183 | AFR | ACB | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02572 | hp1 | a0001 | c0001 | t0014 | g0036 | AFR | GWD | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0117 | AFR | GWD | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0162 | AFR | GWD | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02622 | hp1 | a0001 | c0001 | t0013 | g0173 | AFR | GWD | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02622 | hp2 | a0001 | c0001 | t0022 | g0198 | AFR | GWD | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0139 | SAS | PJL | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02717 | hp1 | a0001 | c0001 | t0020 | g0163 | AFR | GWD | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0201 | AFR | GWD | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0164 | AFR | GWD | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02818 | hp2 | a0001 | c0001 | t0018 | g0127 | AFR | GWD | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0113 | AFR | GWD | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02886 | hp2 | a0001 | c0001 | t0037 | g0193 | AFR | GWD | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0171 | AFR | GWD | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02895 | hp2 | a0001 | c0002 | t0012 | g0035 | AFR | GWD | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0029 | AFR | GWD | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02897 | hp2 | a0001 | c0002 | t0012 | g0035 | AFR | GWD | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02922 | hp1 | a0001 | c0001 | t0006 | g0028 | AFR | ESN | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0125 | AFR | ESN | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0189 | AFR | ESN | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0027 | AFR | ESN | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0120 | AFR | ESN | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02976 | hp2 | a0001 | c0001 | t0006 | g0028 | AFR | ESN | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | MSL | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | MSL | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0129 | AFR | ESN | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0029 | AFR | ESN | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0124 | AFR | ESN | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0126 | AFR | ESN | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG03209 | hp1 | a0001 | c0001 | t0008 | g0180 | AFR | MSL | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0191 | AFR | MSL | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0165 | AFR | MSL | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG03225 | hp2 | a0001 | c0001 | t0013 | g0111 | AFR | MSL | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG03453 | hp1 | a0001 | c0001 | t0040 | g0058 | AFR | MSL | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0187 | AFR | MSL | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | MSL | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG03490 | hp1 | a0001 | c0001 | t0015 | g0031 | SAS | PJL | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0130 | SAS | PJL | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0155 | SAS | PJL | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0151 | SAS | PJL | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG03492 | hp2 | a0001 | c0001 | t0015 | g0031 | SAS | PJL | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0170 | AFR | ESN | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG03516 | hp2 | a0001 | c0001 | t0006 | g0185 | AFR | ESN | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0190 | AFR | GWD | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0112 | AFR | GWD | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0169 | AFR | MSL | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | MSL | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG03654 | hp1 | a0001 | c0001 | t0007 | g0181 | SAS | PJL | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG03654 | hp2 | a0001 | c0001 | t0011 | g0013 | SAS | PJL | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0143 | SAS | PJL | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG03704 | hp2 | a0001 | c0001 | t0045 | g0097 | SAS | PJL | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | BEB | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | BEB | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG04199 | hp1 | a0001 | c0001 | t0011 | g0013 | SAS | STU | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | STU | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | STU | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | STU | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | STU | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG04228 | hp2 | a0001 | c0001 | t0007 | g0182 | SAS | STU | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0168 | AFR | YRI | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18522 | hp2 | a0001 | c0001 | t0010 | g0030 | AFR | YRI | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | CHB | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | CHB | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHB | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | YRI | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | YRI | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18952 | hp2 | a0001 | c0001 | t0016 | g0053 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18970 | hp1 | a0001 | c0001 | t0025 | g0148 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18974 | hp2 | a0001 | c0001 | t0016 | g0052 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18978 | hp1 | a0001 | c0001 | t0034 | g0051 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18982 | hp1 | a0001 | c0001 | t0030 | g0084 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA19003 | hp2 | a0001 | c0001 | t0031 | g0018 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA19004 | hp2 | a0001 | c0001 | t0042 | g0008 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA19007 | hp1 | a0001 | c0001 | t0044 | g0055 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA19007 | hp2 | a0001 | c0001 | t0028 | g0010 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA19030 | hp1 | a0001 | c0001 | t0008 | g0178 | AFR | LWK | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0026 | AFR | LWK | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0200 | AFR | LWK | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA19043 | hp2 | a0001 | c0001 | t0027 | g0184 | AFR | LWK | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA19065 | hp2 | a0001 | c0001 | t0036 | g0018 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA19240 | hp2 | a0001 | c0001 | t0008 | g0179 | AFR | YRI | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ASW | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ASW | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0149 | EUR | TSI | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0042 | EUR | TSI | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | GIH | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0009 | SAS | GIH | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | CLM | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02109 | hp2 | a0001 | c0001 | t0010 | g0197 | AFR | ACB | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02486 | hp1 | a0001 | c0001 | t0021 | g0160 | AFR | ACB | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0027 | AFR | ACB | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02559 | hp1 | a0001 | c0001 | t0010 | g0030 | AFR | ACB | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0167 | AFR | ACB | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG06807 | hp1 | a0001 | c0001 | t0008 | g0174 | AFR | USA | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| HG06807 | hp2 | a0001 | c0001 | t0009 | g0007 | AFR | USA | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA21309 | hp1 | a0001 | c0001 | t0026 | g0119 | AFR | LWK | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| NA21309 | hp2 | a0001 | c0001 | t0006 | g0188 | AFR | LWK | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0038 | REF | REF | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0108 | REF | REF | PCGF5_chr10_91215663_91289337 | PCGF5 | chr10 | 91215663 | 91289337 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:91240500 | T | C | 1 | a0001c0002 | 2 | HG02895.hp2 HG02897.hp2 |
synonymous_variant | LOW | c.129T>C | p.Ile43Ile | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/10 | 486/7149 | 129/771 | 43/256 | chr10 | 91240500 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:91220807 | G | C | 1 | a0001c0001t0018 | 1 | HG02818.hp2 | 5_prime_UTR_variant | MODIFIER | c.-213G>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 1/10 | 2065 | chr10 | 91220807 | ||||||
| chr10:91278488 | G | T | 1 | a0001c0001t0017 | 2 | HG01884.hp2 HG02280.hp2 |
3_prime_UTR_variant | MODIFIER | c.*172G>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 172 | chr10 | 91278488 | ||||||
| chr10:91278697 | T | C | 1 | a0001c0001t0019 | 1 | HG01070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*381T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 381 | chr10 | 91278697 | ||||||
| chr10:91278773 | G | A | 21 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(18): Show |
127 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*457G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 457 | chr10 | 91278773 | ||||||
| chr10:91278935 | G | A | 1 | a0001c0002t0012 | 2 | HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*619G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 619 | chr10 | 91278935 | ||||||
| chr10:91278980 | T | C | 1 | a0001c0001t0028 | 1 | NA19007.hp2 | 3_prime_UTR_variant | MODIFIER | c.*664T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 664 | chr10 | 91278980 | ||||||
| chr10:91279369 | G | A | 1 | a0001c0001t0011 | 4 | HG01255.hp2 HG01884.hp1 HG03654.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1053G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 1053 | chr10 | 91279369 | ||||||
| chr10:91279488 | G | A | 1 | a0001c0001t0029 | 1 | HG01952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1172G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 1172 | chr10 | 91279488 | ||||||
| chr10:91279519 | C | T | 6 | a0001c0001t0006 a0001c0001t0014 a0001c0001t0017 others(3): Show |
14 | HG01081.hp2 HG01884.hp2 HG01891.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1203C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 1203 | chr10 | 91279519 | ||||||
| chr10:91279551 | C | T | 1 | a0001c0001t0045 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1235C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 1235 | chr10 | 91279551 | ||||||
| chr10:91279741 | C | T | 1 | a0001c0001t0013 | 2 | HG02622.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1425C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 1425 | chr10 | 91279741 | ||||||
| chr10:91279819 | G | A | 1 | a0001c0001t0017 | 2 | HG01884.hp2 HG02280.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1503G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 1503 | chr10 | 91279819 | ||||||
| chr10:91279856 | T | G | 1 | a0001c0001t0030 | 1 | NA18982.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1540T>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 1540 | chr10 | 91279856 | ||||||
| chr10:91279999 | T | C | 1 | a0001c0001t0031 | 1 | NA19003.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1683T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 1683 | chr10 | 91279999 | ||||||
| chr10:91280490 | A | C | 1 | a0001c0001t0044 | 1 | NA19007.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2174A>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 2174 | chr10 | 91280490 | ||||||
| chr10:91280592 | G | A | 1 | a0001c0002t0012 | 2 | HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2276G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 2276 | chr10 | 91280592 | ||||||
| chr10:91280691 | C | G | 1 | a0001c0001t0030 | 1 | NA18982.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2375C>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 2375 | chr10 | 91280691 | ||||||
| chr10:91280744 | C | T | 1 | a0001c0001t0008 | 5 | HG02451.hp2 HG03209.hp1 HG06807.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2428C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 2428 | chr10 | 91280744 | ||||||
| chr10:91280747 | G | A | 1 | a0001c0001t0020 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2431G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 2431 | chr10 | 91280747 | ||||||
| chr10:91281013 | G | C | 1 | a0001c0001t0032 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2697G>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 2697 | chr10 | 91281013 | ||||||
| chr10:91281019 | A | G | 1 | a0001c0001t0017 | 2 | HG01884.hp2 HG02280.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2703A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 2703 | chr10 | 91281019 | ||||||
| chr10:91281050 | A | G | 1 | a0001c0001t0027 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2734A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 2734 | chr10 | 91281050 | ||||||
| chr10:91281107 | A | G | 3 | a0001c0001t0014 a0001c0001t0017 a0001c0002t0012 |
6 | HG01884.hp2 HG01891.hp1 HG02280.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2791A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 2791 | chr10 | 91281107 | ||||||
| chr10:91281316 | T | C | 1 | a0001c0001t0005 | 6 | HG01192.hp1 HG02896.hp2 HG02965.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3000T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 3000 | chr10 | 91281316 | ||||||
| chr10:91281335 | C | G | 1 | a0001c0002t0012 | 2 | HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3019C>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 3019 | chr10 | 91281335 | ||||||
| chr10:91281360 | A | T | 1 | a0001c0001t0026 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3044A>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 3044 | chr10 | 91281360 | ||||||
| chr10:91281411 | G | A | 1 | a0001c0001t0033 | 1 | HG01515.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3095G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 3095 | chr10 | 91281411 | ||||||
| chr10:91281556 | T | G | 1 | a0001c0001t0015 | 2 | HG03490.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3240T>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 3240 | chr10 | 91281556 | ||||||
| chr10:91281638 | C | T | 2 | a0001c0001t0004 a0001c0001t0020 |
16 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3322C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 3322 | chr10 | 91281638 | ||||||
| chr10:91281701 | A | G | 1 | a0001c0001t0043 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3385A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 3385 | chr10 | 91281701 | ||||||
| chr10:91281782 | T | G | 1 | a0001c0002t0012 | 2 | HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3466T>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 3466 | chr10 | 91281782 | ||||||
| chr10:91281934 | C | A | 1 | a0001c0001t0016 | 2 | NA18952.hp2 NA18974.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3618C>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 3618 | chr10 | 91281934 | ||||||
| chr10:91281947 | G | C | 1 | a0001c0001t0034 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3631G>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 3631 | chr10 | 91281947 | ||||||
| chr10:91282063 | AGACTTTG others(16): Show |
A | 1 | a0001c0001t0035 | 1 | HG01169.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3748_*3770delGACT others(19): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 3748 | chr10 | 91282063 | ||||||
| chr10:91282086 | C | T | 1 | a0001c0001t0001 | 1 | NA18975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3770C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 3770 | chr10 | 91282086 | ||||||
| chr10:91282112 | T | C | 3 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0013 |
12 | HG00140.hp1 HG01256.hp2 HG01258.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3796T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 3796 | chr10 | 91282112 | ||||||
| chr10:91282206 | C | G | 1 | a0001c0001t0042 | 1 | NA19004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3890C>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 3890 | chr10 | 91282206 | ||||||
| chr10:91282207 | G | A | 3 | a0001c0001t0004 a0001c0001t0020 a0001c0001t0021 |
17 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*3891G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 3891 | chr10 | 91282207 | ||||||
| chr10:91282242 | T | C | 2 | a0001c0001t0031 a0001c0001t0036 |
2 | NA19003.hp2 NA19065.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3926T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 3926 | chr10 | 91282242 | ||||||
| chr10:91282356 | C | T | 2 | a0001c0001t0031 a0001c0001t0036 |
2 | NA19003.hp2 NA19065.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4040C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 4040 | chr10 | 91282356 | ||||||
| chr10:91282494 | T | G | 12 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(9): Show |
43 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*4178T>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 4178 | chr10 | 91282494 | ||||||
| chr10:91282582 | A | C | 1 | a0001c0001t0041 | 1 | HG01256.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4266A>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 4266 | chr10 | 91282582 | ||||||
| chr10:91282591 | C | T | 1 | a0001c0001t0025 | 1 | NA18970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4275C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 4275 | chr10 | 91282591 | ||||||
| chr10:91282672 | A | G | 1 | a0001c0001t0040 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4356A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 4356 | chr10 | 91282672 | ||||||
| chr10:91282678 | T | C | 1 | a0001c0001t0037 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4362T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 4362 | chr10 | 91282678 | ||||||
| chr10:91282721 | G | A | 1 | a0001c0001t0014 | 2 | HG01891.hp1 HG02572.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4405G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 4405 | chr10 | 91282721 | ||||||
| chr10:91282743 | A | G | 1 | a0001c0001t0024 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4427A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 4427 | chr10 | 91282743 | ||||||
| chr10:91283182 | A | G | 1 | a0001c0001t0017 | 2 | HG01884.hp2 HG02280.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4866A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 4866 | chr10 | 91283182 | ||||||
| chr10:91283691 | A | G | 1 | a0001c0001t0026 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5375A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 5375 | chr10 | 91283691 | ||||||
| chr10:91283768 | A | G | 1 | a0001c0001t0010 | 4 | HG02109.hp2 HG02258.hp1 HG02559.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5452A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 5452 | chr10 | 91283768 | ||||||
| chr10:91283866 | A | T | 1 | a0001c0001t0039 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5550A>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 5550 | chr10 | 91283866 | ||||||
| chr10:91284030 | C | T | 1 | a0001c0001t0023 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5714C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 5714 | chr10 | 91284030 | ||||||
| chr10:91284101 | T | C | 4 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0023 others(1): Show |
48 | HG00099.hp1 HG00408.hp2 HG00639.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*5785T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 5785 | chr10 | 91284101 | ||||||
| chr10:91284172 | A | T | 8 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(5): Show |
36 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*5856A>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 5856 | chr10 | 91284172 | ||||||
| chr10:91284175 | C | CT | 4 | a0001c0001t0010 a0001c0001t0022 a0001c0001t0033 others(1): Show |
7 | HG01361.hp1 HG01515.hp1 HG02109.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5870dupT | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 5871 | INFO_REALIGN_3_PRIME | chr10 | 91284175 | |||||
| chr10:91284266 | T | C | 1 | a0001c0002t0012 | 2 | HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5950T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 10/10 | 5950 | chr10 | 91284266 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:91220927 | G | T | 1 | a0001c0002t0012g0035 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-184+91G>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 1/9 | chr10 | 91220927 | |||||||
| chr10:91221016 | C | T | 52 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(49): Show |
75 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.-184+180C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 1/9 | chr10 | 91221016 | |||||||
| chr10:91221169 | G | C | 2 | a0001c0001t0014g0036 a0001c0001t0014g0037 |
2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.-184+333G>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 1/9 | chr10 | 91221169 | |||||||
| chr10:91221193 | C | T | 1 | a0001c0001t0002g0205 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-184+357C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 1/9 | chr10 | 91221193 | |||||||
| chr10:91221435 | A | G | 3 | a0001c0001t0001g0016 a0001c0001t0035g0016 a0001c0001t0041g0016 |
3 | HG01168.hp1 HG01169.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.-184+599A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 1/9 | chr10 | 91221435 | |||||||
| chr10:91221512 | C | T | 2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | HG02135.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.-184+676C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 1/9 | chr10 | 91221512 | |||||||
| chr10:91221627 | C | T | 1 | a0001c0001t0001g0202 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-184+791C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 1/9 | chr10 | 91221627 | |||||||
| chr10:91221680 | A | G | 7 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(4): Show |
8 | HG02109.hp2 HG02145.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-184+844A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 1/9 | chr10 | 91221680 | |||||||
| chr10:91221723 | TA | T | 63 | a0001c0001t0001g0134 a0001c0001t0001g0152 a0001c0001t0002g0003 others(60): Show |
76 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.-184+902delA | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 91221723 | ||||||
| chr10:91221723 | TAA | T | 40 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(37): Show |
45 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.-184+901_-184+902d others(4): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 91221723 | ||||||
| chr10:91221724 | A | T | 1 | a0001c0001t0001g0106 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-184+888A>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 1/9 | chr10 | 91221724 | |||||||
| chr10:91221733 | A | G | 2 | a0001c0001t0003g0194 a0001c0001t0003g0195 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-184+897A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 1/9 | chr10 | 91221733 | |||||||
| chr10:91221734 | A | C | 1 | a0001c0001t0037g0193 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-184+898A>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 1/9 | chr10 | 91221734 | |||||||
| chr10:91221892 | A | C | 1 | a0001c0001t0001g0246 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-183-797A>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 1/9 | chr10 | 91221892 | |||||||
| chr10:91222469 | A | G | 1 | a0001c0001t0001g0034 | 2 | NA18947.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.-183-220A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 1/9 | chr10 | 91222469 | |||||||
| chr10:91222481 | G | A | 38 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(35): Show |
42 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.-183-208G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 1/9 | chr10 | 91222481 | |||||||
| chr10:91222503 | A | G | 2 | a0001c0001t0014g0036 a0001c0001t0014g0037 |
2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.-183-186A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 1/9 | chr10 | 91222503 | |||||||
| chr10:91223151 | G | A | 59 | a0001c0001t0001g0134 a0001c0001t0001g0152 a0001c0001t0002g0003 others(56): Show |
72 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.112+168G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91223151 | |||||||
| chr10:91223178 | C | G | 2 | a0001c0001t0005g0191 a0001c0001t0005g0192 |
2 | HG01192.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.112+195C>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91223178 | |||||||
| chr10:91223215 | A | G | 1 | a0001c0002t0012g0035 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.112+232A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91223215 | |||||||
| chr10:91223376 | C | T | 59 | a0001c0001t0001g0134 a0001c0001t0001g0152 a0001c0001t0002g0003 others(56): Show |
72 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.112+393C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91223376 | |||||||
| chr10:91223646 | T | C | 1 | a0001c0001t0015g0031 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.112+663T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91223646 | |||||||
| chr10:91224074 | A | G | 35 | a0001c0001t0001g0134 a0001c0001t0001g0152 a0001c0001t0002g0003 others(32): Show |
44 | HG00099.hp1 HG00408.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.112+1091A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91224074 | |||||||
| chr10:91224298 | A | G | 18 | a0001c0001t0006g0028 a0001c0001t0006g0185 a0001c0001t0006g0186 others(15): Show |
19 | HG00140.hp1 HG01081.hp2 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.112+1315A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91224298 | |||||||
| chr10:91224370 | A | C | 2 | a0001c0001t0014g0036 a0001c0001t0014g0037 |
2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.112+1387A>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91224370 | |||||||
| chr10:91224396 | T | C | 1 | a0001c0001t0013g0173 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.112+1413T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91224396 | |||||||
| chr10:91224495 | A | AT | 36 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(33): Show |
40 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.112+1516dupT | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr10 | 91224495 | ||||||
| chr10:91224859 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.112+1876A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91224859 | |||||||
| chr10:91224865 | T | A | 1 | a0001c0001t0001g0042 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.112+1882T>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91224865 | |||||||
| chr10:91224877 | A | G | 6 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0243 others(3): Show |
6 | HG01346.hp1 HG01943.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.112+1894A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91224877 | |||||||
| chr10:91224890 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.112+1907G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91224890 | |||||||
| chr10:91224951 | T | G | 2 | a0001c0001t0017g0039 a0001c0001t0017g0040 |
2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.112+1968T>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91224951 | |||||||
| chr10:91224972 | T | C | 1 | a0001c0001t0008g0174 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.112+1989T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91224972 | |||||||
| chr10:91225026 | G | A | 38 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(35): Show |
42 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.112+2043G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91225026 | |||||||
| chr10:91225220 | T | TGATATAT others(43): Show |
1 | a0001c0001t0002g0159 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.112+2254_112+2303d others(52): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr10 | 91225220 | ||||||
| chr10:91225230 | C | CATATATG others(19): Show |
1 | a0001c0001t0001g0109 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.112+2261_112+2286d others(28): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr10 | 91225230 | ||||||
| chr10:91225289 | CATATATA others(6): Show |
C | 1 | a0001c0001t0002g0158 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.112+2324_112+2336d others(15): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr10 | 91225289 | ||||||
| chr10:91225418 | A | G | 3 | a0001c0001t0010g0030 a0001c0001t0010g0196 a0001c0001t0010g0197 |
4 | HG02109.hp2 HG02258.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+2435A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91225418 | |||||||
| chr10:91225502 | A | G | 9 | a0001c0001t0004g0027 a0001c0001t0004g0165 a0001c0001t0004g0166 others(6): Show |
10 | HG02055.hp1 HG02280.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.112+2519A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91225502 | |||||||
| chr10:91225776 | C | T | 2 | a0001c0001t0013g0111 a0001c0001t0013g0173 |
2 | HG02622.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.112+2793C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91225776 | |||||||
| chr10:91226165 | G | A | 1 | a0001c0001t0022g0198 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.112+3182G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91226165 | |||||||
| chr10:91226238 | C | T | 1 | a0001c0001t0003g0129 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.112+3255C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91226238 | |||||||
| chr10:91226255 | T | C | 2 | a0001c0001t0001g0034 a0001c0001t0001g0206 |
3 | NA18947.hp1 NA18978.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.112+3272T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91226255 | |||||||
| chr10:91226289 | T | TA | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(147): Show |
195 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.112+3331dupA | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr10 | 91226289 | ||||||
| chr10:91226289 | T | TAA | 29 | a0001c0001t0001g0017 a0001c0001t0001g0045 a0001c0001t0001g0046 others(26): Show |
30 | HG00140.hp2 HG01109.hp2 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.112+3330_112+3331d others(4): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr10 | 91226289 | ||||||
| chr10:91226289 | T | TAAA | 14 | a0001c0001t0001g0152 a0001c0001t0001g0207 a0001c0001t0002g0015 others(11): Show |
19 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.112+3329_112+3331d others(5): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr10 | 91226289 | ||||||
| chr10:91226289 | T | TAAAA | 22 | a0001c0001t0001g0134 a0001c0001t0002g0003 a0001c0001t0002g0024 others(19): Show |
29 | HG00408.hp2 HG01123.hp2 HG01168.hp2 others(26): Show |
intron_variant | MODIFIER | c.112+3328_112+3331d others(6): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr10 | 91226289 | ||||||
| chr10:91226289 | TA | T | 6 | a0001c0001t0004g0172 a0001c0001t0005g0192 a0001c0001t0006g0028 others(3): Show |
7 | HG01081.hp2 HG01192.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.112+3331delA | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr10 | 91226289 | ||||||
| chr10:91226369 | C | G | 1 | a0001c0002t0012g0035 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.112+3386C>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91226369 | |||||||
| chr10:91226405 | C | T | 3 | a0001c0001t0014g0036 a0001c0001t0014g0037 a0001c0002t0012g0035 |
4 | HG01891.hp1 HG02572.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.112+3422C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91226405 | |||||||
| chr10:91226430 | A | T | 14 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(11): Show |
16 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.112+3447A>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91226430 | |||||||
| chr10:91226456 | T | C | 2 | a0001c0001t0013g0111 a0001c0001t0013g0173 |
2 | HG02622.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.112+3473T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91226456 | |||||||
| chr10:91226514 | A | C | 1 | a0001c0001t0001g0106 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.112+3531A>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91226514 | |||||||
| chr10:91226569 | A | G | 2 | a0001c0001t0014g0036 a0001c0001t0014g0037 |
2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.112+3586A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91226569 | |||||||
| chr10:91226662 | C | T | 1 | a0001c0001t0002g0144 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.112+3679C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91226662 | |||||||
| chr10:91226702 | AG | A | 9 | a0001c0001t0004g0027 a0001c0001t0004g0165 a0001c0001t0004g0166 others(6): Show |
10 | HG02055.hp1 HG02280.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.112+3722delG | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr10 | 91226702 | ||||||
| chr10:91226864 | C | G | 33 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(30): Show |
36 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.112+3881C>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91226864 | |||||||
| chr10:91226864 | C | T | 4 | a0001c0001t0014g0036 a0001c0001t0014g0037 a0001c0001t0017g0040 others(1): Show |
5 | HG01884.hp2 HG01891.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.112+3881C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91226864 | |||||||
| chr10:91226868 | C | T | 1 | a0001c0001t0017g0040 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.112+3885C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91226868 | |||||||
| chr10:91226890 | A | C | 1 | a0001c0001t0037g0193 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.112+3907A>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91226890 | |||||||
| chr10:91227002 | G | T | 1 | a0001c0001t0004g0164 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.112+4019G>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91227002 | |||||||
| chr10:91227194 | T | C | 5 | a0001c0001t0005g0029 a0001c0001t0005g0189 a0001c0001t0005g0190 others(2): Show |
6 | HG01192.hp1 HG02896.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.112+4211T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91227194 | |||||||
| chr10:91227537 | T | C | 1 | a0001c0001t0044g0055 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.112+4554T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91227537 | |||||||
| chr10:91227587 | C | T | 7 | a0001c0001t0003g0041 a0001c0001t0003g0116 a0001c0001t0003g0117 others(4): Show |
7 | HG00639.hp2 HG01109.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.112+4604C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91227587 | |||||||
| chr10:91227637 | A | G | 1 | a0001c0001t0043g0105 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.112+4654A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91227637 | |||||||
| chr10:91227753 | C | T | 31 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(28): Show |
34 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.112+4770C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91227753 | |||||||
| chr10:91227808 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.112+4825T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91227808 | |||||||
| chr10:91228071 | T | C | 1 | a0001c0001t0002g0130 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.112+5088T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91228071 | |||||||
| chr10:91228076 | A | G | 3 | a0001c0001t0010g0030 a0001c0001t0010g0196 a0001c0001t0010g0197 |
4 | HG02109.hp2 HG02258.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+5093A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91228076 | |||||||
| chr10:91228119 | T | G | 2 | a0001c0001t0031g0018 a0001c0001t0036g0018 |
2 | NA19003.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.112+5136T>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91228119 | |||||||
| chr10:91228340 | T | C | 1 | a0001c0001t0001g0056 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.112+5357T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91228340 | |||||||
| chr10:91228424 | A | G | 2 | a0001c0001t0017g0039 a0001c0001t0017g0040 |
2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.112+5441A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91228424 | |||||||
| chr10:91228489 | G | A | 3 | a0001c0001t0010g0030 a0001c0001t0010g0196 a0001c0001t0010g0197 |
4 | HG02109.hp2 HG02258.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+5506G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91228489 | |||||||
| chr10:91228726 | A | G | 12 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(9): Show |
14 | HG01192.hp1 HG02109.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.112+5743A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91228726 | |||||||
| chr10:91228997 | G | A | 2 | a0001c0001t0017g0039 a0001c0001t0017g0040 |
2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.112+6014G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91228997 | |||||||
| chr10:91229238 | T | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0057 a0001c0001t0028g0010 |
4 | NA18747.hp2 NA18975.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.112+6255T>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91229238 | |||||||
| chr10:91229255 | G | A | 3 | a0001c0001t0001g0059 a0001c0001t0001g0109 a0001c0001t0040g0058 |
3 | HG01243.hp2 HG02717.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.112+6272G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91229255 | |||||||
| chr10:91229431 | A | G | 2 | a0001c0001t0014g0036 a0001c0001t0014g0037 |
2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.112+6448A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91229431 | |||||||
| chr10:91229718 | C | A | 1 | a0001c0001t0026g0119 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.112+6735C>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91229718 | |||||||
| chr10:91229767 | C | A | 21 | a0001c0001t0006g0028 a0001c0001t0006g0185 a0001c0001t0006g0186 others(18): Show |
23 | HG00140.hp1 HG01081.hp2 HG01256.hp2 others(20): Show |
intron_variant | MODIFIER | c.112+6784C>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91229767 | |||||||
| chr10:91229831 | A | G | 19 | a0001c0001t0006g0028 a0001c0001t0006g0185 a0001c0001t0006g0186 others(16): Show |
20 | HG00140.hp1 HG01081.hp2 HG01256.hp2 others(17): Show |
intron_variant | MODIFIER | c.112+6848A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91229831 | |||||||
| chr10:91230069 | G | A | 59 | a0001c0001t0001g0134 a0001c0001t0001g0152 a0001c0001t0002g0003 others(56): Show |
72 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.112+7086G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91230069 | |||||||
| chr10:91230351 | A | C | 33 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(30): Show |
36 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.112+7368A>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91230351 | |||||||
| chr10:91230586 | A | C | 2 | a0001c0001t0017g0039 a0001c0001t0017g0040 |
2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.112+7603A>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91230586 | |||||||
| chr10:91230811 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.112+7828C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91230811 | |||||||
| chr10:91230814 | G | T | 1 | a0001c0001t0004g0164 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.112+7831G>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91230814 | |||||||
| chr10:91230826 | T | A | 3 | a0001c0001t0006g0028 a0001c0001t0006g0186 a0001c0001t0006g0187 |
4 | HG01081.hp2 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.112+7843T>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91230826 | |||||||
| chr10:91230846 | C | G | 4 | a0001c0001t0001g0152 a0001c0001t0002g0015 a0001c0001t0002g0153 others(1): Show |
6 | HG00639.hp1 HG00741.hp2 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.112+7863C>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91230846 | |||||||
| chr10:91230876 | A | C | 1 | a0001c0001t0001g0054 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.112+7893A>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91230876 | |||||||
| chr10:91230989 | A | G | 2 | a0001c0001t0017g0039 a0001c0001t0017g0040 |
2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.112+8006A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91230989 | |||||||
| chr10:91231125 | T | G | 1 | a0001c0001t0002g0131 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.112+8142T>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91231125 | |||||||
| chr10:91231153 | T | C | 115 | a0001c0001t0001g0016 a0001c0001t0001g0134 a0001c0001t0001g0152 others(112): Show |
137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.112+8170T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91231153 | |||||||
| chr10:91231231 | G | A | 2 | a0001c0001t0003g0200 a0001c0001t0022g0198 |
2 | HG02622.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.112+8248G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91231231 | |||||||
| chr10:91231529 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.112+8546G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91231529 | |||||||
| chr10:91231696 | G | T | 1 | a0001c0001t0026g0119 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.112+8713G>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91231696 | |||||||
| chr10:91231750 | G | A | 5 | a0001c0001t0007g0175 a0001c0001t0007g0176 a0001c0001t0007g0177 others(2): Show |
5 | HG00140.hp1 HG01256.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.113-8734G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91231750 | |||||||
| chr10:91232055 | G | A | 1 | a0001c0001t0001g0060 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.113-8429G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91232055 | |||||||
| chr10:91232062 | G | A | 1 | a0001c0001t0002g0132 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.113-8422G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91232062 | |||||||
| chr10:91232097 | G | T | 14 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(11): Show |
16 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.113-8387G>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91232097 | |||||||
| chr10:91232188 | G | A | 2 | a0001c0001t0017g0039 a0001c0001t0017g0040 |
2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.113-8296G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91232188 | |||||||
| chr10:91232227 | A | G | 3 | a0001c0001t0017g0039 a0001c0001t0017g0040 a0001c0002t0012g0035 |
4 | HG01884.hp2 HG02280.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.113-8257A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91232227 | |||||||
| chr10:91232575 | A | G | 38 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(35): Show |
42 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.113-7909A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91232575 | |||||||
| chr10:91232621 | T | C | 2 | a0001c0001t0013g0111 a0001c0001t0013g0173 |
2 | HG02622.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.113-7863T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91232621 | |||||||
| chr10:91232773 | A | AGAAAGT | 38 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(35): Show |
42 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.113-7709_113-7708i others(8): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr10 | 91232773 | ||||||
| chr10:91232860 | G | A | 1 | a0001c0001t0001g0061 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.113-7624G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91232860 | |||||||
| chr10:91232881 | G | A | 1 | a0001c0001t0001g0208 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.113-7603G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91232881 | |||||||
| chr10:91233341 | A | G | 2 | a0001c0001t0001g0103 a0001c0001t0001g0104 |
2 | NA18964.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.113-7143A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91233341 | |||||||
| chr10:91233373 | C | T | 1 | a0001c0001t0037g0193 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.113-7111C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91233373 | |||||||
| chr10:91233436 | T | C | 1 | a0001c0001t0008g0174 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.113-7048T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91233436 | |||||||
| chr10:91233464 | C | T | 33 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(30): Show |
36 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.113-7020C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91233464 | |||||||
| chr10:91233529 | C | T | 38 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(35): Show |
42 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.113-6955C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91233529 | |||||||
| chr10:91233632 | C | T | 3 | a0001c0001t0006g0185 a0001c0001t0006g0188 a0001c0001t0021g0160 |
3 | HG02486.hp1 HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.113-6852C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91233632 | |||||||
| chr10:91233643 | A | T | 2 | a0001c0001t0017g0039 a0001c0001t0017g0040 |
2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.113-6841A>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91233643 | |||||||
| chr10:91233984 | T | C | 2 | a0001c0001t0001g0215 a0001c0001t0001g0216 |
2 | HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.113-6500T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91233984 | |||||||
| chr10:91234119 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.113-6365C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91234119 | |||||||
| chr10:91234358 | G | A | 12 | a0001c0001t0007g0175 a0001c0001t0007g0176 a0001c0001t0007g0177 others(9): Show |
12 | HG00140.hp1 HG01256.hp2 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.113-6126G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91234358 | |||||||
| chr10:91234749 | A | G | 1 | a0001c0001t0004g0172 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.113-5735A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91234749 | |||||||
| chr10:91234877 | C | G | 38 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(35): Show |
42 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.113-5607C>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91234877 | |||||||
| chr10:91235181 | C | T | 2 | a0001c0001t0001g0238 a0001c0001t0039g0237 |
2 | HG02056.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.113-5303C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91235181 | |||||||
| chr10:91235260 | C | T | 1 | a0001c0001t0002g0154 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.113-5224C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91235260 | |||||||
| chr10:91235511 | C | G | 3 | a0001c0001t0017g0039 a0001c0001t0017g0040 a0001c0002t0012g0035 |
4 | HG01884.hp2 HG02280.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.113-4973C>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91235511 | |||||||
| chr10:91235521 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.113-4963T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91235521 | |||||||
| chr10:91235677 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.113-4807G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91235677 | |||||||
| chr10:91235750 | A | T | 3 | a0001c0001t0010g0030 a0001c0001t0010g0196 a0001c0001t0010g0197 |
4 | HG02109.hp2 HG02258.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-4734A>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91235750 | |||||||
| chr10:91235823 | A | G | 105 | a0001c0001t0001g0100 a0001c0001t0001g0134 a0001c0001t0001g0152 others(102): Show |
125 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.113-4661A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91235823 | |||||||
| chr10:91236101 | T | TA | 37 | a0001c0001t0001g0207 a0001c0001t0004g0026 a0001c0001t0004g0027 others(34): Show |
41 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.113-4376dupA | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr10 | 91236101 | ||||||
| chr10:91236139 | G | A | 6 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(3): Show |
6 | HG02109.hp2 HG02145.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.113-4345G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91236139 | |||||||
| chr10:91236178 | G | C | 2 | a0001c0001t0008g0178 a0001c0001t0008g0183 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.113-4306G>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91236178 | |||||||
| chr10:91236260 | G | C | 38 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(35): Show |
42 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.113-4224G>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91236260 | |||||||
| chr10:91236305 | G | A | 1 | a0001c0001t0026g0119 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.113-4179G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91236305 | |||||||
| chr10:91236313 | C | T | 49 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(46): Show |
72 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.113-4171C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91236313 | |||||||
| chr10:91236348 | C | A | 50 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(47): Show |
56 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(53): Show |
intron_variant | MODIFIER | c.113-4136C>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91236348 | |||||||
| chr10:91236355 | T | C | 3 | a0001c0001t0006g0185 a0001c0001t0006g0188 a0001c0001t0021g0160 |
3 | HG02486.hp1 HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.113-4129T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91236355 | |||||||
| chr10:91236369 | A | C | 1 | a0001c0001t0009g0044 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.113-4115A>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91236369 | |||||||
| chr10:91236501 | A | G | 1 | a0001c0001t0001g0244 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.113-3983A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91236501 | |||||||
| chr10:91236540 | A | G | 2 | a0001c0001t0016g0052 a0001c0001t0016g0053 |
2 | NA18952.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.113-3944A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91236540 | |||||||
| chr10:91236610 | G | A | 36 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(33): Show |
40 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.113-3874G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91236610 | |||||||
| chr10:91236611 | G | A | 1 | a0001c0001t0001g0219 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.113-3873G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91236611 | |||||||
| chr10:91236701 | T | G | 1 | a0001c0001t0001g0220 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.113-3783T>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91236701 | |||||||
| chr10:91236702 | G | A | 38 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(35): Show |
42 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.113-3782G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91236702 | |||||||
| chr10:91237040 | C | G | 36 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(33): Show |
40 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.113-3444C>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91237040 | |||||||
| chr10:91237170 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.113-3314G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91237170 | |||||||
| chr10:91237217 | A | G | 3 | a0001c0001t0001g0012 a0001c0001t0001g0098 a0001c0001t0001g0099 |
5 | HG00597.hp1 NA18962.hp2 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.113-3267A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91237217 | |||||||
| chr10:91237481 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.113-3003G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91237481 | |||||||
| chr10:91237509 | G | A | 38 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(35): Show |
42 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.113-2975G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91237509 | |||||||
| chr10:91237511 | A | G | 38 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(35): Show |
42 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.113-2973A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91237511 | |||||||
| chr10:91237641 | G | A | 1 | a0001c0002t0012g0035 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.113-2843G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91237641 | |||||||
| chr10:91237693 | G | A | 1 | a0001c0001t0006g0185 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.113-2791G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91237693 | |||||||
| chr10:91237742 | T | TA | 38 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(35): Show |
42 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.113-2728dupA | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr10 | 91237742 | ||||||
| chr10:91237761 | A | T | 1 | a0001c0001t0001g0213 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.113-2723A>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91237761 | |||||||
| chr10:91237964 | C | G | 1 | a0001c0001t0001g0236 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.113-2520C>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91237964 | |||||||
| chr10:91238073 | A | G | 1 | a0001c0001t0006g0187 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.113-2411A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91238073 | |||||||
| chr10:91238082 | A | G | 1 | a0001c0001t0014g0037 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.113-2402A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91238082 | |||||||
| chr10:91238085 | T | C | 1 | a0001c0001t0037g0193 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.113-2399T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91238085 | |||||||
| chr10:91238173 | A | G | 3 | a0001c0001t0002g0143 a0001c0001t0002g0151 a0001c0001t0002g0155 |
3 | HG03491.hp2 HG03492.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.113-2311A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91238173 | |||||||
| chr10:91238241 | A | G | 2 | a0001c0001t0014g0036 a0001c0001t0014g0037 |
2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.113-2243A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91238241 | |||||||
| chr10:91238387 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.113-2097G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91238387 | |||||||
| chr10:91238581 | A | ATTTCTTT others(5): Show |
1 | a0001c0001t0004g0027 | 2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.113-1891_113-1880d others(14): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr10 | 91238581 | ||||||
| chr10:91238581 | A | ATTTCTTT others(9): Show |
1 | a0001c0001t0007g0182 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.113-1895_113-1880d others(18): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr10 | 91238581 | ||||||
| chr10:91238581 | A | ATTTCTTT others(17): Show |
4 | a0001c0001t0007g0175 a0001c0001t0007g0176 a0001c0001t0007g0181 others(1): Show |
4 | HG00140.hp1 HG01258.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-1880_113-1879i others(26): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr10 | 91238581 | ||||||
| chr10:91238581 | A | ATTTCTTT others(21): Show |
3 | a0001c0001t0006g0028 a0001c0001t0008g0179 a0001c0001t0013g0111 |
4 | HG02922.hp1 HG02976.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.113-1880_113-1879i others(30): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr10 | 91238581 | ||||||
| chr10:91238581 | A | ATTTCTTT others(29): Show |
1 | a0001c0001t0008g0174 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.113-1880_113-1879i others(38): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr10 | 91238581 | ||||||
| chr10:91238601 | C | CT | 12 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0021 others(9): Show |
13 | HG00323.hp2 HG01071.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.113-1853dupT | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr10 | 91238601 | ||||||
| chr10:91238601 | CT | C | 58 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(55): Show |
76 | HG00423.hp2 HG00438.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.113-1853delT | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr10 | 91238601 | ||||||
| chr10:91238601 | CTT | C | 41 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(38): Show |
50 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.113-1854_113-1853d others(4): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr10 | 91238601 | ||||||
| chr10:91238601 | CTTT | C | 8 | a0001c0001t0003g0116 a0001c0001t0003g0128 a0001c0001t0005g0029 others(5): Show |
9 | HG00639.hp2 HG01109.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.113-1855_113-1853d others(5): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr10 | 91238601 | ||||||
| chr10:91238601 | CTTTTTT | C | 27 | a0001c0001t0001g0134 a0001c0001t0001g0152 a0001c0001t0002g0003 others(24): Show |
35 | HG00099.hp1 HG00408.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.113-1858_113-1853d others(8): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr10 | 91238601 | ||||||
| chr10:91238601 | CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0002g0143 a0001c0001t0002g0151 a0001c0001t0002g0155 |
3 | HG03491.hp2 HG03492.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.113-1864_113-1853d others(14): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr10 | 91238601 | ||||||
| chr10:91238602 | T | TTTCTTTC others(4): Show |
5 | a0001c0001t0004g0026 a0001c0001t0004g0166 a0001c0001t0004g0169 others(2): Show |
5 | HG02055.hp1 HG02486.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.113-1880_113-1879i others(13): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr10 | 91238602 | ||||||
| chr10:91238602 | T | TTTCTTTC others(8): Show |
2 | a0001c0001t0004g0171 a0001c0001t0006g0186 |
2 | HG01081.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.113-1880_113-1879i others(17): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr10 | 91238602 | ||||||
| chr10:91238602 | T | TTTCTTTC others(12): Show |
2 | a0001c0001t0008g0178 a0001c0001t0008g0183 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.113-1880_113-1879i others(21): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr10 | 91238602 | ||||||
| chr10:91238602 | T | TTTCTTTC others(24): Show |
1 | a0001c0001t0008g0180 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.113-1880_113-1879i others(33): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr10 | 91238602 | ||||||
| chr10:91238602 | T | TTTCTTTC others(40): Show |
1 | a0001c0001t0027g0184 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.113-1880_113-1879i others(49): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr10 | 91238602 | ||||||
| chr10:91238603 | T | TTCTTTCT others(3): Show |
7 | a0001c0001t0004g0026 a0001c0001t0004g0161 a0001c0001t0004g0162 others(4): Show |
7 | HG00735.hp1 HG01243.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.113-1880_113-1879i others(12): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr10 | 91238603 | ||||||
| chr10:91238603 | T | TTCTTTCT others(7): Show |
2 | a0001c0001t0004g0165 a0001c0001t0004g0168 |
2 | HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.113-1880_113-1879i others(16): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr10 | 91238603 | ||||||
| chr10:91238603 | T | TTCTTTCT others(19): Show |
1 | a0001c0001t0007g0177 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.113-1880_113-1879i others(28): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr10 | 91238603 | ||||||
| chr10:91238603 | T | TTCTTTCT others(23): Show |
1 | a0001c0001t0006g0188 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.113-1880_113-1879i others(32): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr10 | 91238603 | ||||||
| chr10:91238604 | T | TCTTTCTT others(26): Show |
1 | a0001c0001t0006g0185 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.113-1880_113-1879i others(35): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91238604 | |||||||
| chr10:91238605 | T | C | 9 | a0001c0001t0006g0028 a0001c0001t0007g0175 a0001c0001t0007g0176 others(6): Show |
10 | HG00140.hp1 HG01258.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.113-1879T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91238605 | |||||||
| chr10:91238606 | T | C | 4 | a0001c0001t0006g0186 a0001c0001t0006g0187 a0001c0001t0008g0180 others(1): Show |
4 | HG01081.hp2 HG03209.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-1878T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91238606 | |||||||
| chr10:91238607 | T | C | 2 | a0001c0001t0006g0188 a0001c0001t0007g0177 |
2 | HG01256.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.113-1877T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91238607 | |||||||
| chr10:91238608 | T | C | 1 | a0001c0001t0006g0185 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.113-1876T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91238608 | |||||||
| chr10:91238609 | T | C | 1 | a0001c0001t0007g0182 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.113-1875T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91238609 | |||||||
| chr10:91238611 | T | C | 1 | a0001c0001t0006g0188 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.113-1873T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91238611 | |||||||
| chr10:91238612 | T | C | 2 | a0001c0001t0006g0185 a0001c0001t0014g0037 |
2 | HG01891.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.113-1872T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91238612 | |||||||
| chr10:91238613 | T | C | 2 | a0001c0001t0014g0036 a0001c0001t0014g0037 |
2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.113-1871T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91238613 | |||||||
| chr10:91238614 | T | C | 1 | a0001c0001t0014g0036 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.113-1870T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91238614 | |||||||
| chr10:91238615 | T | C | 1 | a0001c0001t0006g0188 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.113-1869T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91238615 | |||||||
| chr10:91238632 | G | A | 12 | a0001c0001t0007g0175 a0001c0001t0007g0176 a0001c0001t0007g0177 others(9): Show |
12 | HG00140.hp1 HG01256.hp2 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.113-1852G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91238632 | |||||||
| chr10:91238662 | A | G | 1 | a0001c0001t0007g0182 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.113-1822A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91238662 | |||||||
| chr10:91238779 | T | C | 5 | a0001c0001t0008g0174 a0001c0001t0008g0178 a0001c0001t0008g0179 others(2): Show |
5 | HG02451.hp2 HG03209.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.113-1705T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91238779 | |||||||
| chr10:91238902 | C | A | 14 | a0001c0001t0001g0134 a0001c0001t0002g0003 a0001c0001t0002g0025 others(11): Show |
20 | HG00408.hp2 HG02074.hp2 NA18612.hp2 others(17): Show |
intron_variant | MODIFIER | c.113-1582C>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91238902 | |||||||
| chr10:91238925 | T | A | 2 | a0001c0001t0013g0111 a0001c0001t0013g0173 |
2 | HG02622.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.113-1559T>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91238925 | |||||||
| chr10:91239026 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.113-1458C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91239026 | |||||||
| chr10:91239042 | A | T | 15 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(12): Show |
17 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.113-1442A>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91239042 | |||||||
| chr10:91239109 | C | T | 5 | a0001c0001t0005g0029 a0001c0001t0005g0189 a0001c0001t0005g0190 others(2): Show |
6 | HG01192.hp1 HG02896.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.113-1375C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91239109 | |||||||
| chr10:91239505 | TGAG | T | 3 | a0001c0001t0006g0028 a0001c0001t0006g0186 a0001c0001t0006g0187 |
4 | HG01081.hp2 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.113-975_113-973del others(3): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr10 | 91239505 | ||||||
| chr10:91239718 | G | A | 1 | a0001c0001t0005g0189 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.113-766G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91239718 | |||||||
| chr10:91239897 | G | C | 2 | a0001c0001t0002g0139 a0001c0001t0002g0158 |
2 | HG01175.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.113-587G>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91239897 | |||||||
| chr10:91239957 | A | G | 1 | a0001c0001t0001g0023 | 2 | HG04199.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.113-527A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91239957 | |||||||
| chr10:91240027 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.113-457C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91240027 | |||||||
| chr10:91240047 | T | C | 1 | a0001c0001t0001g0064 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.113-437T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91240047 | |||||||
| chr10:91240150 | CTG | C | 12 | a0001c0001t0007g0175 a0001c0001t0007g0176 a0001c0001t0007g0177 others(9): Show |
12 | HG00140.hp1 HG01256.hp2 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.113-332_113-331del others(2): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr10 | 91240150 | ||||||
| chr10:91240189 | A | C | 15 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(12): Show |
17 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.113-295A>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91240189 | |||||||
| chr10:91240338 | C | T | 1 | a0001c0001t0002g0139 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.113-146C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91240338 | |||||||
| chr10:91240454 | G | A | 159 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(156): Show |
201 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.113-30G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 2/9 | chr10 | 91240454 | |||||||
| chr10:91240650 | G | C | 1 | a0001c0001t0026g0119 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.209+70G>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91240650 | |||||||
| chr10:91240695 | T | G | 1 | a0001c0001t0001g0241 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.209+115T>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91240695 | |||||||
| chr10:91240754 | G | A | 2 | a0001c0001t0017g0039 a0001c0001t0017g0040 |
2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.209+174G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91240754 | |||||||
| chr10:91240899 | G | A | 1 | a0001c0001t0003g0199 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.209+319G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91240899 | |||||||
| chr10:91240912 | A | G | 1 | a0001c0001t0034g0051 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.209+332A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91240912 | |||||||
| chr10:91241042 | C | CAT | 5 | a0001c0001t0005g0029 a0001c0001t0005g0189 a0001c0001t0005g0190 others(2): Show |
6 | HG01192.hp1 HG02896.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.209+474_209+475dup others(2): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr10 | 91241042 | ||||||
| chr10:91241218 | G | A | 2 | a0001c0001t0001g0065 a0001c0001t0001g0107 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.209+638G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91241218 | |||||||
| chr10:91241224 | G | A | 18 | a0001c0001t0006g0028 a0001c0001t0006g0185 a0001c0001t0006g0186 others(15): Show |
19 | HG00140.hp1 HG01081.hp2 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.209+644G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91241224 | |||||||
| chr10:91241318 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.209+738C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91241318 | |||||||
| chr10:91241499 | C | T | 1 | a0001c0001t0027g0184 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.209+919C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91241499 | |||||||
| chr10:91241511 | C | T | 1 | a0001c0001t0002g0150 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.209+931C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91241511 | |||||||
| chr10:91241515 | T | C | 1 | a0001c0001t0002g0133 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.209+935T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91241515 | |||||||
| chr10:91241640 | C | T | 1 | a0001c0001t0003g0125 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.209+1060C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91241640 | |||||||
| chr10:91241743 | T | C | 1 | a0001c0001t0001g0019 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.209+1163T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91241743 | |||||||
| chr10:91241930 | C | T | 1 | a0001c0002t0012g0035 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.209+1350C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91241930 | |||||||
| chr10:91241953 | C | G | 1 | a0001c0001t0001g0214 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.209+1373C>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91241953 | |||||||
| chr10:91241980 | G | A | 4 | a0001c0001t0001g0066 a0001c0001t0001g0068 a0001c0001t0001g0069 others(1): Show |
4 | HG01934.hp2 HG01952.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.209+1400G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91241980 | |||||||
| chr10:91242039 | G | A | 5 | a0001c0001t0005g0029 a0001c0001t0005g0189 a0001c0001t0005g0190 others(2): Show |
6 | HG01192.hp1 HG02896.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.209+1459G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91242039 | |||||||
| chr10:91242143 | T | A | 2 | a0001c0001t0017g0039 a0001c0001t0017g0040 |
2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.209+1563T>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91242143 | |||||||
| chr10:91242419 | T | TA | 38 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(35): Show |
42 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.209+1845dupA | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr10 | 91242419 | ||||||
| chr10:91242563 | G | A | 7 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(4): Show |
8 | HG02109.hp2 HG02145.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.209+1983G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91242563 | |||||||
| chr10:91242727 | A | T | 1 | a0001c0001t0002g0149 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.209+2147A>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91242727 | |||||||
| chr10:91242790 | C | A | 14 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(11): Show |
16 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.209+2210C>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91242790 | |||||||
| chr10:91243041 | T | G | 7 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(4): Show |
8 | HG02109.hp2 HG02145.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.209+2461T>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91243041 | |||||||
| chr10:91243155 | T | A | 1 | a0001c0001t0001g0070 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.209+2575T>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91243155 | |||||||
| chr10:91243335 | T | A | 1 | a0001c0001t0001g0071 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.209+2755T>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91243335 | |||||||
| chr10:91243420 | A | T | 1 | a0001c0001t0010g0030 | 2 | HG02559.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.209+2840A>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91243420 | |||||||
| chr10:91243445 | A | G | 33 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(30): Show |
36 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.209+2865A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91243445 | |||||||
| chr10:91243846 | T | C | 1 | a0001c0001t0027g0184 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.209+3266T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91243846 | |||||||
| chr10:91243896 | A | G | 1 | a0001c0001t0045g0097 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.209+3316A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91243896 | |||||||
| chr10:91243982 | C | G | 1 | a0001c0002t0012g0035 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.209+3402C>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91243982 | |||||||
| chr10:91244087 | AAACCATA others(4): Show |
A | 1 | a0001c0001t0003g0125 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.209+3510_209+3520d others(13): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr10 | 91244087 | ||||||
| chr10:91244259 | A | G | 2 | a0001c0001t0008g0178 a0001c0001t0008g0183 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.209+3679A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91244259 | |||||||
| chr10:91244376 | C | T | 2 | a0001c0001t0014g0036 a0001c0001t0014g0037 |
2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.209+3796C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91244376 | |||||||
| chr10:91244736 | T | C | 1 | a0001c0001t0021g0160 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.210-3769T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91244736 | |||||||
| chr10:91244764 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.210-3741A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91244764 | |||||||
| chr10:91244928 | A | AGTT | 38 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(35): Show |
42 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.210-3576_210-3575i others(5): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr10 | 91244928 | ||||||
| chr10:91244931 | T | C | 1 | a0001c0001t0001g0072 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.210-3574T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91244931 | |||||||
| chr10:91245009 | A | C | 1 | a0001c0001t0004g0170 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.210-3496A>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91245009 | |||||||
| chr10:91245032 | G | A | 1 | a0001c0001t0003g0200 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.210-3473G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91245032 | |||||||
| chr10:91245068 | C | T | 36 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(33): Show |
40 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.210-3437C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91245068 | |||||||
| chr10:91245082 | A | G | 49 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(46): Show |
72 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.210-3423A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91245082 | |||||||
| chr10:91245523 | CTTTAT | C | 33 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(30): Show |
36 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.210-2978_210-2974d others(7): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr10 | 91245523 | ||||||
| chr10:91245527 | A | G | 1 | a0001c0001t0003g0201 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.210-2978A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91245527 | |||||||
| chr10:91245700 | C | T | 94 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0024 others(91): Show |
111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.210-2805C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91245700 | |||||||
| chr10:91245815 | G | A | 3 | a0001c0001t0002g0143 a0001c0001t0002g0151 a0001c0001t0002g0155 |
3 | HG03491.hp2 HG03492.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.210-2690G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91245815 | |||||||
| chr10:91245835 | G | A | 1 | a0001c0001t0003g0120 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.210-2670G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91245835 | |||||||
| chr10:91245846 | C | T | 2 | a0001c0001t0017g0039 a0001c0001t0017g0040 |
2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.210-2659C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91245846 | |||||||
| chr10:91245856 | G | C | 1 | a0001c0001t0010g0030 | 2 | HG02559.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.210-2649G>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91245856 | |||||||
| chr10:91245989 | G | A | 2 | a0001c0001t0031g0018 a0001c0001t0036g0018 |
2 | NA19003.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.210-2516G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91245989 | |||||||
| chr10:91246127 | T | A | 38 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(35): Show |
42 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.210-2378T>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91246127 | |||||||
| chr10:91246337 | A | G | 3 | a0001c0001t0007g0175 a0001c0001t0007g0176 a0001c0001t0007g0177 |
3 | HG00140.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.210-2168A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91246337 | |||||||
| chr10:91246406 | T | C | 1 | a0001c0001t0001g0246 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.210-2099T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91246406 | |||||||
| chr10:91246660 | T | C | 3 | a0001c0001t0017g0039 a0001c0001t0017g0040 a0001c0002t0012g0035 |
4 | HG01884.hp2 HG02280.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.210-1845T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91246660 | |||||||
| chr10:91246794 | C | T | 1 | a0001c0001t0008g0178 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.210-1711C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91246794 | |||||||
| chr10:91246801 | A | G | 2 | a0001c0001t0014g0036 a0001c0001t0014g0037 |
2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.210-1704A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91246801 | |||||||
| chr10:91246945 | AGATAGAT others(5): Show |
A | 4 | a0001c0001t0001g0012 a0001c0001t0001g0099 a0001c0001t0002g0140 others(1): Show |
4 | HG00099.hp1 HG00597.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.210-1552_210-1541d others(14): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr10 | 91246945 | ||||||
| chr10:91246957 | GGATAGAT others(13): Show |
G | 1 | a0001c0001t0001g0103 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.210-1540_210-1521d others(22): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr10 | 91246957 | ||||||
| chr10:91246965 | GGATA | G | 44 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(41): Show |
59 | HG00323.hp2 HG00741.hp1 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.210-1487_210-1484d others(6): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr10 | 91246965 | ||||||
| chr10:91246965 | GGATAGAT others(1): Show |
G | 101 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(98): Show |
112 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.210-1491_210-1484d others(10): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr10 | 91246965 | ||||||
| chr10:91246965 | GGATAGAT others(5): Show |
G | 96 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(93): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.210-1495_210-1484d others(14): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr10 | 91246965 | ||||||
| chr10:91246965 | GGATAGAT others(9): Show |
G | 9 | a0001c0001t0001g0063 a0001c0001t0001g0098 a0001c0001t0003g0121 others(6): Show |
9 | HG01256.hp2 HG01258.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.210-1499_210-1484d others(18): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr10 | 91246965 | ||||||
| chr10:91246965 | GGATAGAT others(13): Show |
G | 3 | a0001c0001t0001g0004 a0001c0001t0001g0059 a0001c0001t0001g0062 |
3 | HG00621.hp1 HG01243.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.210-1503_210-1484d others(22): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr10 | 91246965 | ||||||
| chr10:91246965 | GGATAGAT others(21): Show |
G | 2 | a0001c0001t0013g0111 a0001c0001t0013g0173 |
2 | HG02622.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.210-1511_210-1484d others(30): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr10 | 91246965 | ||||||
| chr10:91246973 | A | G | 4 | a0001c0001t0001g0012 a0001c0001t0001g0099 a0001c0001t0002g0140 others(1): Show |
4 | HG00099.hp1 HG00597.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.210-1532A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91246973 | |||||||
| chr10:91246981 | A | G | 3 | a0001c0001t0003g0200 a0001c0001t0010g0196 a0001c0001t0010g0197 |
3 | HG02109.hp2 HG02258.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.210-1524A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91246981 | |||||||
| chr10:91247247 | C | A | 14 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(11): Show |
16 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.210-1258C>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91247247 | |||||||
| chr10:91247410 | T | C | 1 | a0001c0001t0001g0221 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.210-1095T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91247410 | |||||||
| chr10:91247427 | T | G | 1 | a0001c0001t0001g0073 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.210-1078T>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91247427 | |||||||
| chr10:91247452 | A | G | 1 | a0001c0001t0001g0234 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.210-1053A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91247452 | |||||||
| chr10:91247593 | G | C | 1 | a0001c0001t0001g0071 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.210-912G>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91247593 | |||||||
| chr10:91247815 | G | T | 1 | a0001c0001t0008g0180 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.210-690G>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91247815 | |||||||
| chr10:91247868 | G | T | 3 | a0001c0001t0017g0039 a0001c0001t0017g0040 a0001c0002t0012g0035 |
4 | HG01884.hp2 HG02280.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.210-637G>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91247868 | |||||||
| chr10:91248026 | T | C | 38 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(35): Show |
42 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.210-479T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91248026 | |||||||
| chr10:91248210 | G | A | 1 | a0001c0001t0008g0174 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.210-295G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91248210 | |||||||
| chr10:91248220 | G | A | 43 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(40): Show |
61 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.210-285G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91248220 | |||||||
| chr10:91248307 | G | T | 38 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(35): Show |
42 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.210-198G>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91248307 | |||||||
| chr10:91248420 | G | A | 38 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(35): Show |
42 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.210-85G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91248420 | |||||||
| chr10:91248455 | A | C | 1 | a0001c0001t0002g0205 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.210-50A>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 3/9 | chr10 | 91248455 | |||||||
| chr10:91248600 | A | G | 1 | a0001c0001t0006g0185 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.265+40A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 4/9 | chr10 | 91248600 | |||||||
| chr10:91248880 | G | C | 1 | a0001c0001t0003g0116 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.325+156G>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 5/9 | chr10 | 91248880 | |||||||
| chr10:91249041 | T | G | 2 | a0001c0001t0006g0188 a0001c0001t0021g0160 |
2 | HG02486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.325+317T>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 5/9 | chr10 | 91249041 | |||||||
| chr10:91249092 | G | A | 1 | a0001c0001t0003g0126 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.325+368G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 5/9 | chr10 | 91249092 | |||||||
| chr10:91249371 | GTATA | G | 3 | a0001c0001t0001g0074 a0001c0001t0005g0029 a0001c0001t0005g0189 |
4 | HG01943.hp1 HG02896.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.325+693_325+696del others(4): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr10 | 91249371 | ||||||
| chr10:91249371 | GTATATAT others(1): Show |
G | 3 | a0001c0001t0001g0047 a0001c0001t0001g0075 a0001c0001t0001g0106 |
3 | HG00323.hp2 HG03491.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.325+689_325+696del others(8): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr10 | 91249371 | ||||||
| chr10:91249371 | GTATATAT others(3): Show |
G | 4 | a0001c0001t0001g0066 a0001c0001t0001g0239 a0001c0001t0031g0018 others(1): Show |
4 | HG01993.hp1 NA18950.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.325+687_325+696del others(10): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr10 | 91249371 | ||||||
| chr10:91249371 | GTATATAT others(5): Show |
G | 20 | a0001c0001t0001g0011 a0001c0001t0001g0048 a0001c0001t0001g0063 others(17): Show |
23 | HG00280.hp2 HG01071.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.325+685_325+696del others(12): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr10 | 91249371 | ||||||
| chr10:91249371 | GTATATAT others(7): Show |
G | 45 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0021 others(42): Show |
54 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.325+683_325+696del others(14): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr10 | 91249371 | ||||||
| chr10:91249371 | GTATATAT others(9): Show |
G | 59 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0054 others(56): Show |
68 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.325+681_325+696del others(16): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr10 | 91249371 | ||||||
| chr10:91249371 | GTATATAT others(13): Show |
G | 13 | a0001c0001t0001g0023 a0001c0001t0001g0050 a0001c0001t0001g0096 others(10): Show |
15 | HG00597.hp2 HG01255.hp1 HG02074.hp1 others(12): Show |
intron_variant | MODIFIER | c.325+677_325+696del others(20): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr10 | 91249371 | ||||||
| chr10:91249371 | GTATATAT others(15): Show |
G | 46 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(43): Show |
69 | HG00423.hp2 HG00438.hp1 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.325+675_325+696del others(22): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr10 | 91249371 | ||||||
| chr10:91249371 | GTATATAT others(17): Show |
G | 3 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0238 |
3 | HG02056.hp2 NA18964.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.325+673_325+696del others(24): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr10 | 91249371 | ||||||
| chr10:91249410 | T | C | 5 | a0001c0001t0014g0036 a0001c0001t0014g0037 a0001c0001t0017g0039 others(2): Show |
6 | HG01884.hp2 HG01891.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.325+686T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 5/9 | chr10 | 91249410 | |||||||
| chr10:91249412 | T | C | 33 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(30): Show |
36 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.325+688T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 5/9 | chr10 | 91249412 | |||||||
| chr10:91249581 | A | G | 2 | a0001c0001t0004g0162 a0001c0001t0020g0163 |
2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.325+857A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 5/9 | chr10 | 91249581 | |||||||
| chr10:91249628 | A | C | 1 | a0001c0001t0004g0166 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.325+904A>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 5/9 | chr10 | 91249628 | |||||||
| chr10:91249645 | C | T | 38 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(35): Show |
42 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.325+921C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 5/9 | chr10 | 91249645 | |||||||
| chr10:91249777 | T | TAAC | 15 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(12): Show |
17 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.325+1065_325+1067d others(5): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr10 | 91249777 | ||||||
| chr10:91249789 | C | A | 2 | a0001c0001t0017g0039 a0001c0001t0017g0040 |
2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.325+1065C>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 5/9 | chr10 | 91249789 | |||||||
| chr10:91250022 | G | A | 3 | a0001c0001t0001g0224 a0001c0001t0014g0036 a0001c0001t0014g0037 |
3 | HG00438.hp1 HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.326-1270G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 5/9 | chr10 | 91250022 | |||||||
| chr10:91250176 | T | C | 1 | a0001c0001t0002g0135 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.326-1116T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 5/9 | chr10 | 91250176 | |||||||
| chr10:91250179 | A | G | 1 | a0001c0002t0012g0035 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.326-1113A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 5/9 | chr10 | 91250179 | |||||||
| chr10:91250339 | G | A | 1 | a0001c0001t0003g0112 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.326-953G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 5/9 | chr10 | 91250339 | |||||||
| chr10:91250357 | A | G | 1 | a0001c0001t0008g0180 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.326-935A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 5/9 | chr10 | 91250357 | |||||||
| chr10:91250486 | T | C | 2 | a0001c0001t0001g0021 a0001c0001t0001g0081 |
3 | NA18939.hp1 NA19005.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.326-806T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 5/9 | chr10 | 91250486 | |||||||
| chr10:91250497 | C | CT | 71 | a0001c0001t0001g0006 a0001c0001t0001g0071 a0001c0001t0001g0208 others(68): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.326-779dupT | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr10 | 91250497 | ||||||
| chr10:91250497 | C | CTT | 37 | a0001c0001t0003g0117 a0001c0001t0003g0118 a0001c0001t0004g0026 others(34): Show |
40 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.326-780_326-779dup others(2): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr10 | 91250497 | ||||||
| chr10:91250598 | T | G | 1 | a0001c0001t0021g0160 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.326-694T>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 5/9 | chr10 | 91250598 | |||||||
| chr10:91250626 | G | A | 109 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0024 others(106): Show |
131 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.326-666G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 5/9 | chr10 | 91250626 | |||||||
| chr10:91250699 | A | G | 38 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(35): Show |
42 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.326-593A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 5/9 | chr10 | 91250699 | |||||||
| chr10:91250732 | A | C | 7 | a0001c0001t0006g0028 a0001c0001t0006g0185 a0001c0001t0006g0186 others(4): Show |
8 | HG01081.hp2 HG02486.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.326-560A>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 5/9 | chr10 | 91250732 | |||||||
| chr10:91250913 | C | CTT | 158 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(155): Show |
202 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.326-379_326-378ins others(2): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 5/9 | chr10 | 91250913 | |||||||
| chr10:91250929 | A | G | 2 | a0001c0001t0014g0036 a0001c0001t0014g0037 |
2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.326-363A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 5/9 | chr10 | 91250929 | |||||||
| chr10:91250969 | G | C | 1 | a0001c0001t0002g0141 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.326-323G>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 5/9 | chr10 | 91250969 | |||||||
| chr10:91251097 | AT | A | 8 | a0001c0001t0001g0057 a0001c0001t0001g0069 a0001c0001t0001g0076 others(5): Show |
8 | HG01071.hp2 HG01891.hp1 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.326-177delT | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr10 | 91251097 | ||||||
| chr10:91251097 | ATT | A | 36 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(33): Show |
40 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.326-178_326-177del others(2): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr10 | 91251097 | ||||||
| chr10:91251100 | T | A | 19 | a0001c0001t0006g0028 a0001c0001t0006g0185 a0001c0001t0006g0186 others(16): Show |
20 | HG00140.hp1 HG01081.hp2 HG01256.hp2 others(17): Show |
intron_variant | MODIFIER | c.326-192T>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 5/9 | chr10 | 91251100 | |||||||
| chr10:91251266 | A | T | 1 | a0001c0002t0012g0035 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.326-26A>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 5/9 | chr10 | 91251266 | |||||||
| chr10:91251820 | C | G | 2 | a0001c0001t0001g0043 a0001c0001t0045g0097 |
2 | HG01978.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.474+380C>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91251820 | |||||||
| chr10:91251984 | G | C | 33 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0024 others(30): Show |
42 | HG00099.hp1 HG00408.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.474+544G>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91251984 | |||||||
| chr10:91252013 | A | C | 57 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0024 others(54): Show |
70 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.474+573A>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91252013 | |||||||
| chr10:91252074 | T | G | 1 | a0001c0001t0001g0228 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.474+634T>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91252074 | |||||||
| chr10:91252102 | T | C | 33 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(30): Show |
36 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.474+662T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91252102 | |||||||
| chr10:91252191 | C | T | 38 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(35): Show |
42 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.474+751C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91252191 | |||||||
| chr10:91252352 | G | C | 2 | a0001c0001t0016g0052 a0001c0001t0016g0053 |
2 | NA18952.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.474+912G>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91252352 | |||||||
| chr10:91252375 | T | G | 15 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(12): Show |
17 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.474+935T>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91252375 | |||||||
| chr10:91252404 | A | G | 2 | a0001c0001t0014g0036 a0001c0001t0014g0037 |
2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.474+964A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91252404 | |||||||
| chr10:91252454 | C | G | 2 | a0001c0001t0003g0199 a0001c0001t0003g0201 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.474+1014C>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91252454 | |||||||
| chr10:91252528 | C | G | 38 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(35): Show |
42 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.474+1088C>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91252528 | |||||||
| chr10:91252735 | C | T | 1 | a0001c0001t0001g0054 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.474+1295C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91252735 | |||||||
| chr10:91252777 | G | C | 1 | a0001c0001t0001g0090 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.474+1337G>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91252777 | |||||||
| chr10:91252798 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.474+1358C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91252798 | |||||||
| chr10:91252848 | G | A | 2 | a0001c0001t0004g0162 a0001c0001t0020g0163 |
2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.474+1408G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91252848 | |||||||
| chr10:91252915 | C | A | 5 | a0001c0001t0014g0036 a0001c0001t0014g0037 a0001c0001t0017g0039 others(2): Show |
6 | HG01884.hp2 HG01891.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.474+1475C>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91252915 | |||||||
| chr10:91253003 | A | G | 1 | a0001c0001t0001g0072 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.474+1563A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91253003 | |||||||
| chr10:91253038 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.474+1598T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91253038 | |||||||
| chr10:91253048 | G | T | 1 | a0001c0001t0001g0233 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.474+1608G>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91253048 | |||||||
| chr10:91253107 | A | G | 1 | a0001c0001t0001g0089 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.474+1667A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91253107 | |||||||
| chr10:91253211 | G | T | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(186): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.474+1771G>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91253211 | |||||||
| chr10:91253259 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.474+1819C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91253259 | |||||||
| chr10:91253275 | C | T | 6 | a0001c0001t0006g0028 a0001c0001t0006g0185 a0001c0001t0006g0186 others(3): Show |
7 | HG01081.hp2 HG02922.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.474+1835C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91253275 | |||||||
| chr10:91253288 | G | A | 161 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(158): Show |
206 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.474+1848G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91253288 | |||||||
| chr10:91253326 | G | T | 38 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(35): Show |
42 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.474+1886G>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91253326 | |||||||
| chr10:91253354 | GCCT | G | 5 | a0001c0001t0005g0029 a0001c0001t0005g0189 a0001c0001t0005g0190 others(2): Show |
6 | HG01192.hp1 HG02896.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.474+1916_474+1918d others(5): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr10 | 91253354 | ||||||
| chr10:91253360 | T | C | 38 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(35): Show |
42 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.474+1920T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91253360 | |||||||
| chr10:91253603 | G | A | 5 | a0001c0001t0007g0175 a0001c0001t0007g0176 a0001c0001t0007g0177 others(2): Show |
5 | HG00140.hp1 HG01256.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.474+2163G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91253603 | |||||||
| chr10:91253605 | G | A | 6 | a0001c0001t0002g0024 a0001c0001t0002g0139 a0001c0001t0002g0141 others(3): Show |
7 | HG01123.hp2 HG01168.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.474+2165G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91253605 | |||||||
| chr10:91253619 | G | T | 12 | a0001c0001t0007g0175 a0001c0001t0007g0176 a0001c0001t0007g0177 others(9): Show |
12 | HG00140.hp1 HG01256.hp2 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.474+2179G>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91253619 | |||||||
| chr10:91253628 | T | G | 1 | a0001c0001t0027g0184 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.474+2188T>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91253628 | |||||||
| chr10:91253724 | G | A | 51 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(48): Show |
74 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.474+2284G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91253724 | |||||||
| chr10:91253764 | C | T | 2 | a0001c0001t0001g0065 a0001c0001t0001g0107 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.474+2324C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91253764 | |||||||
| chr10:91254001 | A | G | 1 | a0001c0001t0001g0049 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.474+2561A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91254001 | |||||||
| chr10:91254076 | C | A | 38 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(35): Show |
42 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.474+2636C>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91254076 | |||||||
| chr10:91254203 | C | CGT | 64 | a0001c0001t0001g0032 a0001c0001t0001g0083 a0001c0001t0002g0003 others(61): Show |
82 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.474+2790_474+2791d others(4): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr10 | 91254203 | ||||||
| chr10:91254203 | C | CGTGT | 8 | a0001c0001t0001g0022 a0001c0001t0001g0047 a0001c0001t0001g0078 others(5): Show |
9 | HG00323.hp1 HG01884.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.474+2788_474+2791d others(6): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr10 | 91254203 | ||||||
| chr10:91254203 | C | CGTGTGT | 18 | a0001c0001t0004g0026 a0001c0001t0004g0161 a0001c0001t0004g0162 others(15): Show |
20 | HG00140.hp1 HG00735.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.474+2786_474+2791d others(8): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr10 | 91254203 | ||||||
| chr10:91254203 | C | CGTGTGTG others(1): Show |
11 | a0001c0001t0004g0027 a0001c0001t0004g0167 a0001c0001t0004g0169 others(8): Show |
12 | HG01081.hp2 HG01884.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.474+2784_474+2791d others(10): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr10 | 91254203 | ||||||
| chr10:91254203 | C | CGTGTGTG others(3): Show |
7 | a0001c0001t0006g0028 a0001c0001t0006g0185 a0001c0001t0006g0187 others(4): Show |
8 | HG02486.hp1 HG02922.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.474+2782_474+2791d others(12): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr10 | 91254203 | ||||||
| chr10:91254203 | C | CGTGTGTG others(5): Show |
1 | a0001c0001t0013g0111 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.474+2780_474+2791d others(14): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr10 | 91254203 | ||||||
| chr10:91254400 | C | T | 2 | a0001c0001t0017g0039 a0001c0001t0017g0040 |
2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.474+2960C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91254400 | |||||||
| chr10:91254745 | A | G | 2 | a0001c0001t0008g0179 a0001c0001t0008g0180 |
2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.474+3305A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91254745 | |||||||
| chr10:91254878 | T | C | 2 | a0001c0001t0017g0039 a0001c0001t0017g0040 |
2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.474+3438T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91254878 | |||||||
| chr10:91254921 | G | T | 2 | a0001c0001t0007g0176 a0001c0001t0007g0177 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.474+3481G>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91254921 | |||||||
| chr10:91255185 | G | A | 1 | a0001c0001t0007g0182 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.474+3745G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91255185 | |||||||
| chr10:91255196 | A | C | 15 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(12): Show |
17 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.474+3756A>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91255196 | |||||||
| chr10:91255322 | T | A | 35 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0024 others(32): Show |
47 | HG00099.hp1 HG00408.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.474+3882T>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91255322 | |||||||
| chr10:91255444 | G | T | 1 | a0001c0001t0003g0199 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.474+4004G>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91255444 | |||||||
| chr10:91255644 | C | T | 38 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(35): Show |
42 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.474+4204C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91255644 | |||||||
| chr10:91255804 | C | A | 38 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(35): Show |
42 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.474+4364C>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91255804 | |||||||
| chr10:91255907 | T | G | 2 | a0001c0001t0014g0036 a0001c0001t0014g0037 |
2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.474+4467T>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91255907 | |||||||
| chr10:91255961 | G | A | 38 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(35): Show |
42 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.474+4521G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91255961 | |||||||
| chr10:91256101 | A | G | 15 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(12): Show |
17 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.474+4661A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91256101 | |||||||
| chr10:91256222 | A | C | 1 | a0001c0001t0017g0040 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.474+4782A>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91256222 | |||||||
| chr10:91256313 | T | G | 33 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(30): Show |
36 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.474+4873T>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91256313 | |||||||
| chr10:91256458 | G | A | 1 | a0001c0002t0012g0035 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.475-4868G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91256458 | |||||||
| chr10:91256859 | AG | A | 14 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(11): Show |
16 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.475-4465delG | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr10 | 91256859 | ||||||
| chr10:91256959 | A | G | 2 | a0001c0001t0017g0039 a0001c0001t0017g0040 |
2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.475-4367A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91256959 | |||||||
| chr10:91256968 | G | C | 26 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(23): Show |
32 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(29): Show |
intron_variant | MODIFIER | c.475-4358G>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91256968 | |||||||
| chr10:91257071 | C | G | 2 | a0001c0001t0014g0036 a0001c0001t0014g0037 |
2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.475-4255C>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91257071 | |||||||
| chr10:91257097 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.475-4229T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91257097 | |||||||
| chr10:91257140 | G | A | 18 | a0001c0001t0006g0028 a0001c0001t0006g0185 a0001c0001t0006g0186 others(15): Show |
19 | HG00140.hp1 HG01081.hp2 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.475-4186G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91257140 | |||||||
| chr10:91257154 | TAA | T | 12 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(9): Show |
14 | HG01192.hp1 HG02109.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.475-4170_475-4169d others(4): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr10 | 91257154 | ||||||
| chr10:91257158 | C | T | 12 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(9): Show |
14 | HG01192.hp1 HG02109.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.475-4168C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91257158 | |||||||
| chr10:91257368 | T | A | 5 | a0001c0001t0014g0036 a0001c0001t0014g0037 a0001c0001t0017g0039 others(2): Show |
6 | HG01884.hp2 HG01891.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.475-3958T>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91257368 | |||||||
| chr10:91257493 | AG | A | 33 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(30): Show |
36 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.475-3829delG | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr10 | 91257493 | ||||||
| chr10:91257516 | G | A | 14 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(11): Show |
16 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.475-3810G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91257516 | |||||||
| chr10:91257555 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.475-3771A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91257555 | |||||||
| chr10:91257837 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.475-3489A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91257837 | |||||||
| chr10:91257844 | A | C | 1 | a0001c0001t0026g0119 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.475-3482A>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91257844 | |||||||
| chr10:91258004 | G | C | 33 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(30): Show |
36 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.475-3322G>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91258004 | |||||||
| chr10:91258288 | A | C | 162 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(159): Show |
204 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.475-3038A>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91258288 | |||||||
| chr10:91258314 | A | G | 39 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(36): Show |
43 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.475-3012A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91258314 | |||||||
| chr10:91258362 | G | C | 1 | a0001c0001t0026g0119 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.475-2964G>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91258362 | |||||||
| chr10:91258482 | C | T | 1 | a0001c0001t0001g0099 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.475-2844C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91258482 | |||||||
| chr10:91258582 | TGCTAA | T | 5 | a0001c0001t0005g0029 a0001c0001t0005g0189 a0001c0001t0005g0190 others(2): Show |
6 | HG01192.hp1 HG02896.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.475-2743_475-2739d others(7): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91258582 | |||||||
| chr10:91258660 | G | A | 3 | a0001c0001t0001g0048 a0001c0001t0001g0076 a0001c0001t0001g0079 |
3 | HG02896.hp1 HG02897.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.475-2666G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91258660 | |||||||
| chr10:91258682 | T | C | 34 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(31): Show |
37 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.475-2644T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91258682 | |||||||
| chr10:91258721 | G | A | 4 | a0001c0001t0003g0200 a0001c0001t0010g0196 a0001c0001t0010g0197 others(1): Show |
4 | HG02109.hp2 HG02258.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.475-2605G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91258721 | |||||||
| chr10:91258784 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.475-2542C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91258784 | |||||||
| chr10:91258836 | T | A | 1 | a0001c0001t0001g0098 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.475-2490T>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91258836 | |||||||
| chr10:91258960 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.475-2366A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91258960 | |||||||
| chr10:91259015 | C | T | 34 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(31): Show |
37 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.475-2311C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91259015 | |||||||
| chr10:91259115 | G | C | 7 | a0001c0001t0008g0174 a0001c0001t0008g0178 a0001c0001t0008g0179 others(4): Show |
7 | HG02451.hp2 HG02622.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.475-2211G>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91259115 | |||||||
| chr10:91259567 | G | C | 39 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(36): Show |
43 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.475-1759G>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91259567 | |||||||
| chr10:91259598 | C | T | 12 | a0001c0001t0007g0175 a0001c0001t0007g0176 a0001c0001t0007g0177 others(9): Show |
12 | HG00140.hp1 HG01256.hp2 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.475-1728C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91259598 | |||||||
| chr10:91259664 | C | T | 2 | a0001c0001t0017g0039 a0001c0001t0017g0040 |
2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.475-1662C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91259664 | |||||||
| chr10:91259714 | T | C | 2 | a0001c0001t0010g0196 a0001c0001t0010g0197 |
2 | HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.475-1612T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91259714 | |||||||
| chr10:91259768 | T | G | 39 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(36): Show |
43 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.475-1558T>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91259768 | |||||||
| chr10:91259881 | A | G | 7 | a0001c0001t0003g0041 a0001c0001t0003g0116 a0001c0001t0003g0117 others(4): Show |
7 | HG00639.hp2 HG01109.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.475-1445A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91259881 | |||||||
| chr10:91259891 | G | T | 26 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(23): Show |
32 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(29): Show |
intron_variant | MODIFIER | c.475-1435G>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91259891 | |||||||
| chr10:91259939 | G | A | 3 | a0001c0001t0003g0117 a0001c0001t0003g0118 a0001c0001t0018g0127 |
3 | HG01433.hp2 HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.475-1387G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91259939 | |||||||
| chr10:91259941 | T | C | 39 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(36): Show |
43 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.475-1385T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91259941 | |||||||
| chr10:91260047 | A | C | 2 | a0001c0001t0014g0036 a0001c0001t0014g0037 |
2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.475-1279A>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91260047 | |||||||
| chr10:91260116 | C | CAAGAAAA others(56): Show |
5 | a0001c0001t0014g0036 a0001c0001t0014g0037 a0001c0001t0017g0039 others(2): Show |
6 | HG01884.hp2 HG01891.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.475-1193_475-1192i others(65): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr10 | 91260116 | ||||||
| chr10:91260116 | C | CAAGAAAA others(56): Show |
20 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(17): Show |
23 | HG00735.hp1 HG01081.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.475-1193_475-1192i others(65): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr10 | 91260116 | ||||||
| chr10:91260116 | C | CAAGAAAA others(56): Show |
14 | a0001c0001t0006g0185 a0001c0001t0006g0188 a0001c0001t0007g0175 others(11): Show |
14 | HG00140.hp1 HG01256.hp2 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.475-1193_475-1192i others(65): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr10 | 91260116 | ||||||
| chr10:91260183 | A | T | 2 | a0001c0001t0008g0178 a0001c0001t0008g0183 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.475-1143A>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91260183 | |||||||
| chr10:91260201 | T | C | 37 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(34): Show |
41 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.475-1125T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91260201 | |||||||
| chr10:91260464 | A | G | 2 | a0001c0001t0013g0111 a0001c0001t0013g0173 |
2 | HG02622.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.475-862A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91260464 | |||||||
| chr10:91260709 | G | C | 1 | a0001c0001t0001g0082 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.475-617G>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91260709 | |||||||
| chr10:91260819 | G | C | 1 | a0001c0001t0004g0167 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.475-507G>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91260819 | |||||||
| chr10:91260865 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.475-461C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91260865 | |||||||
| chr10:91260954 | CATA | C | 41 | a0001c0001t0001g0032 a0001c0001t0001g0225 a0001c0001t0004g0026 others(38): Show |
46 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.475-352_475-350del others(3): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr10 | 91260954 | ||||||
| chr10:91261003 | A | G | 1 | a0001c0001t0001g0227 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.475-323A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91261003 | |||||||
| chr10:91261033 | T | TTTTAA | 39 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(36): Show |
43 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.475-292_475-288dup others(5): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr10 | 91261033 | ||||||
| chr10:91261163 | T | A | 2 | a0001c0001t0017g0039 a0001c0001t0017g0040 |
2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.475-163T>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 6/9 | chr10 | 91261163 | |||||||
| chr10:91261565 | C | T | 1 | a0001c0001t0002g0153 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.573+141C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 7/9 | chr10 | 91261565 | |||||||
| chr10:91261596 | G | A | 39 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(36): Show |
43 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.573+172G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 7/9 | chr10 | 91261596 | |||||||
| chr10:91261623 | A | G | 1 | a0001c0001t0001g0023 | 2 | HG04199.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.573+199A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 7/9 | chr10 | 91261623 | |||||||
| chr10:91261835 | A | G | 1 | a0001c0001t0002g0149 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.573+411A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 7/9 | chr10 | 91261835 | |||||||
| chr10:91261853 | G | A | 34 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(31): Show |
37 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.573+429G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 7/9 | chr10 | 91261853 | |||||||
| chr10:91261887 | T | C | 39 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(36): Show |
43 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.573+463T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 7/9 | chr10 | 91261887 | |||||||
| chr10:91261999 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.573+575G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 7/9 | chr10 | 91261999 | |||||||
| chr10:91262001 | A | C | 5 | a0001c0001t0005g0029 a0001c0001t0005g0189 a0001c0001t0005g0190 others(2): Show |
6 | HG01192.hp1 HG02896.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.573+577A>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 7/9 | chr10 | 91262001 | |||||||
| chr10:91262014 | TAG | T | 2 | a0001c0001t0004g0026 a0001c0001t0004g0164 |
3 | HG01243.hp1 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.573+593_573+594del others(2): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr10 | 91262014 | ||||||
| chr10:91262121 | G | A | 14 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(11): Show |
16 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.573+697G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 7/9 | chr10 | 91262121 | |||||||
| chr10:91262190 | G | T | 39 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(36): Show |
43 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.573+766G>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 7/9 | chr10 | 91262190 | |||||||
| chr10:91262235 | G | T | 1 | a0001c0001t0026g0119 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.573+811G>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 7/9 | chr10 | 91262235 | |||||||
| chr10:91262295 | A | G | 39 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(36): Show |
43 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.573+871A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 7/9 | chr10 | 91262295 | |||||||
| chr10:91262362 | A | G | 2 | a0001c0001t0017g0039 a0001c0001t0017g0040 |
2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.573+938A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 7/9 | chr10 | 91262362 | |||||||
| chr10:91262626 | CTTATTTG others(5): Show |
C | 1 | a0001c0002t0012g0035 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.573+1205_573+1216d others(14): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr10 | 91262626 | ||||||
| chr10:91262927 | A | T | 1 | a0001c0002t0012g0035 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.573+1503A>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 7/9 | chr10 | 91262927 | |||||||
| chr10:91263010 | G | A | 1 | a0001c0001t0002g0136 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.574-1421G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 7/9 | chr10 | 91263010 | |||||||
| chr10:91263237 | G | A | 1 | a0001c0001t0001g0019 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.574-1194G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 7/9 | chr10 | 91263237 | |||||||
| chr10:91263315 | T | TAAAG | 39 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(36): Show |
43 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.574-1113_574-1112i others(6): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr10 | 91263315 | ||||||
| chr10:91263442 | C | CA | 6 | a0001c0001t0001g0033 a0001c0001t0001g0134 a0001c0001t0001g0209 others(3): Show |
7 | HG00597.hp2 HG02071.hp1 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.574-987dupA | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr10 | 91263442 | ||||||
| chr10:91263462 | C | T | 1 | a0001c0001t0002g0159 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.574-969C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 7/9 | chr10 | 91263462 | |||||||
| chr10:91263808 | G | T | 1 | a0001c0001t0001g0075 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.574-623G>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 7/9 | chr10 | 91263808 | |||||||
| chr10:91263861 | G | A | 1 | a0001c0001t0001g0226 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.574-570G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 7/9 | chr10 | 91263861 | |||||||
| chr10:91264109 | A | G | 1 | a0001c0001t0037g0193 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.574-322A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 7/9 | chr10 | 91264109 | |||||||
| chr10:91264169 | T | A | 1 | a0001c0001t0026g0119 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.574-262T>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 7/9 | chr10 | 91264169 | |||||||
| chr10:91264559 | T | TA | 39 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(36): Show |
43 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.663+40dupA | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr10 | 91264559 | ||||||
| chr10:91264838 | A | C | 1 | a0001c0001t0001g0089 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.663+318A>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91264838 | |||||||
| chr10:91264885 | T | G | 1 | a0001c0001t0001g0229 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.663+365T>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91264885 | |||||||
| chr10:91265357 | C | A | 2 | a0001c0001t0001g0230 a0001c0001t0001g0234 |
2 | NA18945.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.663+837C>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91265357 | |||||||
| chr10:91265377 | A | G | 1 | a0001c0001t0001g0023 | 2 | HG04199.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.663+857A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91265377 | |||||||
| chr10:91265429 | T | C | 1 | a0001c0001t0043g0105 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.663+909T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91265429 | |||||||
| chr10:91265434 | G | A | 1 | a0001c0001t0001g0020 | 2 | HG01123.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.663+914G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91265434 | |||||||
| chr10:91265532 | T | C | 1 | a0001c0001t0002g0146 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.663+1012T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91265532 | |||||||
| chr10:91265532 | TA | T | 39 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(36): Show |
43 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.663+1021delA | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr10 | 91265532 | ||||||
| chr10:91265841 | C | T | 3 | a0001c0001t0001g0048 a0001c0001t0001g0076 a0001c0001t0001g0079 |
3 | HG02896.hp1 HG02897.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.663+1321C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91265841 | |||||||
| chr10:91265917 | G | C | 39 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(36): Show |
43 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.663+1397G>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91265917 | |||||||
| chr10:91265920 | A | G | 2 | a0001c0001t0010g0196 a0001c0001t0010g0197 |
2 | HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.663+1400A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91265920 | |||||||
| chr10:91265937 | A | G | 1 | a0001c0001t0010g0030 | 2 | HG02559.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.663+1417A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91265937 | |||||||
| chr10:91266292 | A | G | 2 | a0001c0001t0017g0039 a0001c0001t0017g0040 |
2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.663+1772A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91266292 | |||||||
| chr10:91266529 | T | C | 39 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(36): Show |
43 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.663+2009T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91266529 | |||||||
| chr10:91266561 | GA | G | 3 | a0001c0001t0014g0036 a0001c0001t0014g0037 a0001c0002t0012g0035 |
4 | HG01891.hp1 HG02572.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.663+2046delA | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr10 | 91266561 | ||||||
| chr10:91266783 | T | C | 1 | a0001c0001t0001g0083 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.663+2263T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91266783 | |||||||
| chr10:91266849 | C | G | 1 | a0001c0001t0001g0062 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.663+2329C>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91266849 | |||||||
| chr10:91266859 | C | A | 3 | a0001c0001t0014g0036 a0001c0001t0014g0037 a0001c0002t0012g0035 |
4 | HG01891.hp1 HG02572.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.663+2339C>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91266859 | |||||||
| chr10:91266888 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.663+2368G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91266888 | |||||||
| chr10:91266959 | C | A | 34 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(31): Show |
37 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.663+2439C>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91266959 | |||||||
| chr10:91266959 | C | T | 1 | a0001c0002t0012g0035 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.663+2439C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91266959 | |||||||
| chr10:91267060 | A | G | 5 | a0001c0001t0005g0029 a0001c0001t0005g0189 a0001c0001t0005g0190 others(2): Show |
6 | HG01192.hp1 HG02896.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.663+2540A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91267060 | |||||||
| chr10:91267134 | T | A | 2 | a0001c0001t0014g0036 a0001c0001t0014g0037 |
2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.663+2614T>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91267134 | |||||||
| chr10:91267239 | T | G | 59 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0024 others(56): Show |
75 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.663+2719T>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91267239 | |||||||
| chr10:91267424 | G | A | 1 | a0001c0001t0030g0084 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.663+2904G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91267424 | |||||||
| chr10:91267462 | A | G | 1 | a0001c0001t0002g0149 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.663+2942A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91267462 | |||||||
| chr10:91267505 | G | T | 6 | a0001c0001t0006g0028 a0001c0001t0006g0185 a0001c0001t0006g0186 others(3): Show |
7 | HG01081.hp2 HG02922.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.663+2985G>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91267505 | |||||||
| chr10:91267696 | T | G | 39 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(36): Show |
43 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.663+3176T>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91267696 | |||||||
| chr10:91268488 | G | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0207 a0001c0001t0001g0212 others(5): Show |
13 | HG02109.hp1 HG02257.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.664-3150G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91268488 | |||||||
| chr10:91268511 | T | C | 7 | a0001c0001t0006g0028 a0001c0001t0006g0185 a0001c0001t0006g0186 others(4): Show |
8 | HG01081.hp2 HG02486.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.664-3127T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91268511 | |||||||
| chr10:91268790 | C | T | 2 | a0001c0001t0017g0039 a0001c0001t0017g0040 |
2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.664-2848C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91268790 | |||||||
| chr10:91268927 | G | A | 39 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(36): Show |
43 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.664-2711G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91268927 | |||||||
| chr10:91269283 | T | C | 1 | a0001c0001t0008g0174 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.664-2355T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91269283 | |||||||
| chr10:91269284 | G | A | 2 | a0001c0001t0017g0039 a0001c0001t0017g0040 |
2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.664-2354G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91269284 | |||||||
| chr10:91269614 | T | G | 34 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(31): Show |
37 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.664-2024T>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91269614 | |||||||
| chr10:91270008 | T | C | 1 | a0001c0001t0026g0119 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.664-1630T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91270008 | |||||||
| chr10:91270132 | A | T | 1 | a0001c0001t0003g0114 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.664-1506A>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91270132 | |||||||
| chr10:91270267 | C | G | 1 | a0001c0001t0001g0152 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.664-1371C>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91270267 | |||||||
| chr10:91270380 | G | GA | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(193): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.664-1246dupA | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr10 | 91270380 | ||||||
| chr10:91270421 | A | G | 3 | a0001c0001t0014g0036 a0001c0001t0014g0037 a0001c0002t0012g0035 |
4 | HG01891.hp1 HG02572.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.664-1217A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91270421 | |||||||
| chr10:91270451 | C | T | 39 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(36): Show |
43 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.664-1187C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91270451 | |||||||
| chr10:91270477 | C | T | 1 | a0001c0001t0008g0179 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.664-1161C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91270477 | |||||||
| chr10:91270540 | C | A | 1 | a0001c0001t0003g0114 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.664-1098C>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91270540 | |||||||
| chr10:91270646 | T | G | 1 | a0001c0001t0003g0114 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.664-992T>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91270646 | |||||||
| chr10:91270737 | A | G | 2 | a0001c0001t0008g0179 a0001c0001t0008g0180 |
2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.664-901A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91270737 | |||||||
| chr10:91270787 | A | G | 1 | a0001c0001t0001g0223 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.664-851A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91270787 | |||||||
| chr10:91271103 | T | TATATATA others(11): Show |
15 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(12): Show |
17 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.664-523_664-506dup others(18): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr10 | 91271103 | ||||||
| chr10:91271104 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.664-534A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91271104 | |||||||
| chr10:91271105 | T | TATATATA others(9): Show |
24 | a0001c0001t0006g0028 a0001c0001t0006g0185 a0001c0001t0006g0186 others(21): Show |
26 | HG00140.hp1 HG01081.hp2 HG01256.hp2 others(23): Show |
intron_variant | MODIFIER | c.664-518_664-503dup others(16): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr10 | 91271105 | ||||||
| chr10:91271129 | T | A | 1 | a0001c0001t0003g0114 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.664-509T>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91271129 | |||||||
| chr10:91271200 | G | A | 5 | a0001c0001t0007g0175 a0001c0001t0007g0176 a0001c0001t0007g0177 others(2): Show |
5 | HG00140.hp1 HG01256.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.664-438G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91271200 | |||||||
| chr10:91271239 | C | T | 26 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(23): Show |
28 | HG00140.hp1 HG00735.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.664-399C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91271239 | |||||||
| chr10:91271309 | G | A | 12 | a0001c0001t0007g0175 a0001c0001t0007g0176 a0001c0001t0007g0177 others(9): Show |
12 | HG00140.hp1 HG01256.hp2 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.664-329G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91271309 | |||||||
| chr10:91271446 | A | C | 12 | a0001c0001t0007g0175 a0001c0001t0007g0176 a0001c0001t0007g0177 others(9): Show |
12 | HG00140.hp1 HG01256.hp2 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.664-192A>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91271446 | |||||||
| chr10:91271493 | A | G | 1 | a0001c0002t0012g0035 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.664-145A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91271493 | |||||||
| chr10:91271525 | A | G | 34 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(31): Show |
37 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.664-113A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91271525 | |||||||
| chr10:91271540 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.664-98G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 8/9 | chr10 | 91271540 | |||||||
| chr10:91271728 | C | A | 1 | a0001c0001t0039g0237 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.723+31C>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91271728 | |||||||
| chr10:91271745 | G | A | 12 | a0001c0001t0007g0175 a0001c0001t0007g0176 a0001c0001t0007g0177 others(9): Show |
12 | HG00140.hp1 HG01256.hp2 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.723+48G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91271745 | |||||||
| chr10:91271823 | C | A | 1 | a0001c0001t0001g0054 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.723+126C>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91271823 | |||||||
| chr10:91271848 | T | C | 1 | a0001c0002t0012g0035 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.723+151T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91271848 | |||||||
| chr10:91271920 | T | C | 15 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(12): Show |
17 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.723+223T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91271920 | |||||||
| chr10:91271929 | A | C | 6 | a0001c0001t0003g0014 a0001c0001t0003g0112 a0001c0001t0003g0113 others(3): Show |
8 | HG02257.hp2 HG02258.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.723+232A>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91271929 | |||||||
| chr10:91272174 | C | A | 1 | a0001c0001t0001g0243 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.723+477C>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91272174 | |||||||
| chr10:91272250 | T | A | 39 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(36): Show |
43 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.723+553T>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91272250 | |||||||
| chr10:91272481 | TA | T | 37 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(34): Show |
41 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.723+785delA | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91272481 | |||||||
| chr10:91272482 | A | T | 2 | a0001c0001t0013g0111 a0001c0001t0013g0173 |
2 | HG02622.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.723+785A>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91272482 | |||||||
| chr10:91272497 | A | G | 1 | a0001c0001t0001g0087 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.723+800A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91272497 | |||||||
| chr10:91272544 | G | A | 34 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(31): Show |
37 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.723+847G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91272544 | |||||||
| chr10:91272679 | G | A | 2 | a0001c0001t0017g0039 a0001c0001t0017g0040 |
2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.723+982G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91272679 | |||||||
| chr10:91272700 | G | A | 7 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(4): Show |
8 | HG02109.hp2 HG02145.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.723+1003G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91272700 | |||||||
| chr10:91272754 | C | T | 2 | a0001c0001t0001g0209 a0001c0001t0001g0239 |
2 | NA18950.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.723+1057C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91272754 | |||||||
| chr10:91273186 | C | T | 108 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0024 others(105): Show |
127 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.723+1489C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91273186 | |||||||
| chr10:91273256 | A | G | 46 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(43): Show |
64 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.723+1559A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91273256 | |||||||
| chr10:91273403 | T | C | 1 | a0001c0002t0012g0035 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.723+1706T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91273403 | |||||||
| chr10:91273467 | T | C | 12 | a0001c0001t0007g0175 a0001c0001t0007g0176 a0001c0001t0007g0177 others(9): Show |
12 | HG00140.hp1 HG01256.hp2 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.723+1770T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91273467 | |||||||
| chr10:91273650 | T | C | 5 | a0001c0001t0007g0175 a0001c0001t0007g0176 a0001c0001t0007g0177 others(2): Show |
5 | HG00140.hp1 HG01256.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.723+1953T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91273650 | |||||||
| chr10:91273706 | T | C | 2 | a0001c0001t0017g0039 a0001c0001t0017g0040 |
2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.723+2009T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91273706 | |||||||
| chr10:91273840 | T | C | 1 | a0001c0001t0034g0051 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.723+2143T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91273840 | |||||||
| chr10:91273882 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.723+2185A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91273882 | |||||||
| chr10:91273937 | A | G | 2 | a0001c0001t0014g0036 a0001c0001t0014g0037 |
2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.723+2240A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91273937 | |||||||
| chr10:91273945 | T | C | 1 | a0001c0002t0012g0035 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.723+2248T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91273945 | |||||||
| chr10:91274117 | G | GTA | 35 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(32): Show |
39 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.723+2430_723+2431d others(4): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr10 | 91274117 | ||||||
| chr10:91274136 | T | C | 7 | a0001c0001t0006g0028 a0001c0001t0006g0185 a0001c0001t0006g0186 others(4): Show |
8 | HG01081.hp2 HG02486.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.723+2439T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91274136 | |||||||
| chr10:91274160 | A | G | 1 | a0001c0001t0001g0002 | 7 | NA18939.hp2 NA18959.hp1 NA18961.hp1 others(4): Show |
intron_variant | MODIFIER | c.723+2463A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91274160 | |||||||
| chr10:91274168 | C | G | 1 | a0001c0001t0003g0114 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.723+2471C>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91274168 | |||||||
| chr10:91274556 | G | A | 39 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(36): Show |
43 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.723+2859G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91274556 | |||||||
| chr10:91274599 | C | A | 1 | a0001c0001t0001g0060 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.723+2902C>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91274599 | |||||||
| chr10:91274610 | T | A | 1 | a0001c0001t0003g0114 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.723+2913T>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91274610 | |||||||
| chr10:91274671 | A | G | 39 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(36): Show |
43 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.723+2974A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91274671 | |||||||
| chr10:91274728 | T | C | 3 | a0001c0001t0014g0036 a0001c0001t0014g0037 a0001c0002t0012g0035 |
4 | HG01891.hp1 HG02572.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.723+3031T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91274728 | |||||||
| chr10:91274785 | C | T | 2 | a0001c0001t0017g0039 a0001c0001t0017g0040 |
2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.723+3088C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91274785 | |||||||
| chr10:91274985 | A | G | 6 | a0001c0001t0006g0028 a0001c0001t0006g0185 a0001c0001t0006g0186 others(3): Show |
7 | HG01081.hp2 HG02922.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.724-3284A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91274985 | |||||||
| chr10:91275052 | G | A | 2 | a0001c0001t0001g0092 a0001c0001t0004g0161 |
2 | HG00735.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.724-3217G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91275052 | |||||||
| chr10:91275127 | T | C | 1 | a0001c0001t0022g0198 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.724-3142T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91275127 | |||||||
| chr10:91275307 | GA | G | 48 | a0001c0001t0001g0010 a0001c0001t0001g0057 a0001c0001t0001g0062 others(45): Show |
53 | HG00140.hp1 HG00621.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.724-2953delA | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr10 | 91275307 | ||||||
| chr10:91275445 | A | AT | 41 | a0001c0001t0001g0046 a0001c0001t0001g0202 a0001c0001t0002g0003 others(38): Show |
53 | HG00099.hp1 HG00408.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.724-2810dupT | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr10 | 91275445 | ||||||
| chr10:91275445 | AT | A | 42 | a0001c0001t0001g0048 a0001c0001t0001g0076 a0001c0001t0001g0079 others(39): Show |
46 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.724-2810delT | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr10 | 91275445 | ||||||
| chr10:91275451 | T | A | 39 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(36): Show |
43 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.724-2818T>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91275451 | |||||||
| chr10:91275486 | G | A | 3 | a0001c0001t0003g0123 a0001c0001t0003g0194 a0001c0001t0003g0195 |
3 | HG01169.hp1 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.724-2783G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91275486 | |||||||
| chr10:91275526 | C | T | 14 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(11): Show |
16 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.724-2743C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91275526 | |||||||
| chr10:91275579 | T | C | 5 | a0001c0001t0005g0029 a0001c0001t0005g0189 a0001c0001t0005g0190 others(2): Show |
6 | HG01192.hp1 HG02896.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.724-2690T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91275579 | |||||||
| chr10:91275607 | A | AT | 70 | a0001c0001t0001g0207 a0001c0001t0002g0003 a0001c0001t0002g0015 others(67): Show |
87 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.724-2643dupT | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr10 | 91275607 | ||||||
| chr10:91275607 | A | ATT | 26 | a0001c0001t0002g0133 a0001c0001t0002g0137 a0001c0001t0002g0142 others(23): Show |
29 | HG00140.hp2 HG00735.hp1 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.724-2644_724-2643d others(4): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr10 | 91275607 | ||||||
| chr10:91275607 | AT | A | 7 | a0001c0001t0001g0081 a0001c0001t0001g0086 a0001c0001t0001g0093 others(4): Show |
8 | HG02015.hp1 HG02895.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.724-2643delT | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr10 | 91275607 | ||||||
| chr10:91275607 | ATT | A | 26 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(23): Show |
32 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(29): Show |
intron_variant | MODIFIER | c.724-2644_724-2643d others(4): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr10 | 91275607 | ||||||
| chr10:91275645 | G | A | 1 | a0001c0001t0010g0030 | 2 | HG02559.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.724-2624G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91275645 | |||||||
| chr10:91275654 | C | T | 2 | a0001c0001t0017g0039 a0001c0001t0017g0040 |
2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.724-2615C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91275654 | |||||||
| chr10:91275733 | G | A | 1 | a0001c0002t0012g0035 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.724-2536G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91275733 | |||||||
| chr10:91275745 | G | A | 1 | a0001c0001t0026g0119 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.724-2524G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91275745 | |||||||
| chr10:91275836 | G | A | 39 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(36): Show |
43 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.724-2433G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91275836 | |||||||
| chr10:91276010 | C | T | 2 | a0001c0001t0014g0036 a0001c0001t0014g0037 |
2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.724-2259C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91276010 | |||||||
| chr10:91276105 | G | GA | 13 | a0001c0001t0001g0206 a0001c0001t0003g0114 a0001c0001t0006g0028 others(10): Show |
14 | HG00140.hp2 HG01081.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.724-2153dupA | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr10 | 91276105 | ||||||
| chr10:91276105 | G | GAA | 26 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(23): Show |
29 | HG00140.hp1 HG00735.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.724-2154_724-2153d others(4): Show |
PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr10 | 91276105 | ||||||
| chr10:91276379 | T | C | 7 | a0001c0001t0006g0028 a0001c0001t0006g0185 a0001c0001t0006g0186 others(4): Show |
8 | HG01081.hp2 HG02486.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.724-1890T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91276379 | |||||||
| chr10:91276478 | T | G | 33 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(30): Show |
36 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.724-1791T>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91276478 | |||||||
| chr10:91276634 | G | C | 39 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(36): Show |
43 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.724-1635G>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91276634 | |||||||
| chr10:91276665 | A | C | 39 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(36): Show |
43 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.724-1604A>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91276665 | |||||||
| chr10:91276958 | A | T | 39 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(36): Show |
43 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.724-1311A>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91276958 | |||||||
| chr10:91277189 | T | C | 5 | a0001c0001t0005g0029 a0001c0001t0005g0189 a0001c0001t0005g0190 others(2): Show |
6 | HG01192.hp1 HG02896.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.724-1080T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91277189 | |||||||
| chr10:91277225 | C | T | 39 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(36): Show |
43 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.724-1044C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91277225 | |||||||
| chr10:91277275 | T | A | 3 | a0001c0001t0006g0185 a0001c0001t0006g0188 a0001c0001t0027g0184 |
3 | HG03516.hp2 NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.724-994T>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91277275 | |||||||
| chr10:91277306 | C | T | 1 | a0001c0001t0008g0174 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.724-963C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91277306 | |||||||
| chr10:91277307 | G | A | 2 | a0001c0001t0017g0039 a0001c0001t0017g0040 |
2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.724-962G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91277307 | |||||||
| chr10:91277323 | G | A | 1 | a0001c0001t0001g0088 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.724-946G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91277323 | |||||||
| chr10:91277412 | A | G | 39 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(36): Show |
43 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.724-857A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91277412 | |||||||
| chr10:91277414 | A | G | 39 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(36): Show |
43 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.724-855A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91277414 | |||||||
| chr10:91277420 | T | C | 1 | a0001c0001t0003g0117 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.724-849T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91277420 | |||||||
| chr10:91277560 | T | C | 2 | a0001c0001t0017g0039 a0001c0001t0017g0040 |
2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.724-709T>C | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91277560 | |||||||
| chr10:91277612 | C | T | 9 | a0001c0001t0004g0027 a0001c0001t0004g0165 a0001c0001t0004g0166 others(6): Show |
10 | HG02055.hp1 HG02280.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.724-657C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91277612 | |||||||
| chr10:91277652 | A | G | 34 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0024 others(31): Show |
43 | HG00099.hp1 HG00408.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.724-617A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91277652 | |||||||
| chr10:91277853 | A | G | 57 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0024 others(54): Show |
70 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.724-416A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91277853 | |||||||
| chr10:91277891 | G | A | 3 | a0001c0001t0001g0016 a0001c0001t0035g0016 a0001c0001t0041g0016 |
3 | HG01168.hp1 HG01169.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.724-378G>A | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91277891 | |||||||
| chr10:91278050 | A | G | 8 | a0001c0001t0006g0028 a0001c0001t0006g0185 a0001c0001t0006g0186 others(5): Show |
9 | HG01081.hp2 HG02486.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.724-219A>G | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91278050 | |||||||
| chr10:91278067 | C | T | 39 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0161 others(36): Show |
43 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.724-202C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91278067 | |||||||
| chr10:91278160 | C | T | 2 | a0001c0001t0017g0039 a0001c0001t0017g0040 |
2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.724-109C>T | PCGF5 | ENSG00000180628.15 | transcript | ENST00000336126.6 | protein_coding | 9/9 | chr10 | 91278160 |