Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 80262 |
| ensemblid | ENSG00000125149.12 |
| hgncid | 29564 |
| symbol | PHAF1 |
| name | phagosome assembly factor 1 |
| refseq_nuc | NM_025187.5 |
| refseq_prot | NP_079463.2 |
| ensembl_nuc | ENST00000219139.8 |
| ensembl_prot | ENSP00000219139.3 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 67109941 |
| end | 67148544 |
| strand | + |
| ver | v1.2 |
| region | chr16:67109941-67148544 |
| region5000 | chr16:67104941-67153544 |
| regionname0 | PHAF1_chr16_67109941_67148544 |
| regionname5000 | PHAF1_chr16_67104941_67153544 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 422 | 226 | 91 | 29 | 70 | 10 | 24 | 46 | PHAF1_chr16_67104941_67153544 | PHAF1 | MLDLE others(417): Show |
chr16 | 67104941 | 67153544 |
| a0002 | 0/0 | 422 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | MLDLE others(417): Show |
chr16 | 67104941 | 67153544 |
| a0003 | 0/0 | 422 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | MLDLE others(417): Show |
chr16 | 67104941 | 67153544 |
| a0004 | 0/0 | 422 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | MLDLE others(417): Show |
chr16 | 67104941 | 67153544 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1266 | 226 | 91 | 29 | 70 | 10 | 24 | PHAF1_chr16_67104941_67153544 | PHAF1 | ATGCT others(1261): Show |
chr16 | 67104941 | 67153544 | ||
| a0002c0002 | 0/0 | 1266 | 2 | 0 | 1 | 0 | 0 | 1 | PHAF1_chr16_67104941_67153544 | PHAF1 | ATGCT others(1261): Show |
chr16 | 67104941 | 67153544 | ||
| a0003c0003 | 0/0 | 1266 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | ATGCT others(1261): Show |
chr16 | 67104941 | 67153544 | ||
| a0004c0004 | 0/0 | 1266 | 1 | 0 | 0 | 0 | 0 | 1 | PHAF1_chr16_67104941_67153544 | PHAF1 | ATGCT others(1261): Show |
chr16 | 67104941 | 67153544 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2917 | 150 | 75 | 14 | 40 | 6 | 15 | PHAF1_chr16_67104941_67153544 | PHAF1 | GCAGT others(2912): Show |
chr16 | 67104941 | 67153544 |
| a0001c0001t0002 | 1/1 | 2917 | 62 | 4 | 14 | 30 | 4 | 8 | PHAF1_chr16_67104941_67153544 | PHAF1 | GCAGT others(2912): Show |
chr16 | 67104941 | 67153544 |
| a0001c0001t0003 | 0/0 | 2917 | 11 | 11 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | GCAGT others(2912): Show |
chr16 | 67104941 | 67153544 |
| a0001c0001t0004 | 0/0 | 2917 | 1 | 0 | 1 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | GCAGT others(2912): Show |
chr16 | 67104941 | 67153544 |
| a0001c0001t0005 | 0/0 | 2917 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | GCAGT others(2912): Show |
chr16 | 67104941 | 67153544 |
| a0001c0001t0006 | 0/0 | 2917 | 1 | 0 | 0 | 0 | 0 | 1 | PHAF1_chr16_67104941_67153544 | PHAF1 | GCAGT others(2912): Show |
chr16 | 67104941 | 67153544 |
| a0002c0002t0001 | 0/0 | 2917 | 2 | 0 | 1 | 0 | 0 | 1 | PHAF1_chr16_67104941_67153544 | PHAF1 | GCAGT others(2912): Show |
chr16 | 67104941 | 67153544 |
| a0003c0003t0001 | 0/0 | 2917 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | GCAGT others(2912): Show |
chr16 | 67104941 | 67153544 |
| a0004c0004t0001 | 0/0 | 2917 | 1 | 0 | 0 | 0 | 0 | 1 | PHAF1_chr16_67104941_67153544 | PHAF1 | GCAGT others(2912): Show |
chr16 | 67104941 | 67153544 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0001 | 1/0 | 6 | 0 | 1 | 4 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0002 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0004 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0067 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0003g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0004g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0005g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0001c0001t0006g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0003c0003t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| a0004c0004t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0203 | EUR | GBR | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0043 | EUR | GBR | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | CHS | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0083 | AMR | PUR | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | CHS | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | CHS | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0022 | AMR | PUR | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0081 | AMR | PUR | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | PUR | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0051 | AMR | PUR | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0101 | AMR | PUR | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0075 | AMR | PUR | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0093 | AMR | PUR | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0103 | AMR | PUR | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0110 | AMR | CLM | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0102 | AMR | CLM | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0013 | EUR | IBS | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0034 | EUR | IBS | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0090 | EUR | IBS | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0196 | AFR | ACB | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | PEL | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0091 | AMR | PEL | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | KHV | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | KHV | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | KHV | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | CDX | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | CDX | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0087 | AFR | ACB | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | PEL | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0098 | SAS | PJL | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0193 | AFR | GWD | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0197 | AFR | GWD | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0195 | AFR | GWD | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0194 | AFR | GWD | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02922 | hp2 | a0003 | c0003 | t0001 | g0164 | AFR | ESN | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | ESN | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0117 | AFR | ESN | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ESN | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | ESN | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | MSL | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | MSL | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | MSL | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0100 | SAS | PJL | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0192 | AFR | MSL | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | MSL | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG03491 | hp2 | a0004 | c0004 | t0001 | g0089 | SAS | PJL | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0190 | AFR | ESN | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | GWD | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | MSL | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0097 | SAS | PJL | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | STU | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | STU | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | BEB | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | BEB | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0094 | SAS | BEB | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | BEB | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | STU | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | STU | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | BEB | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0118 | SAS | BEB | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0066 | SAS | STU | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG04199 | hp2 | a0001 | c0001 | t0006 | g0180 | SAS | STU | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | YRI | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | YRI | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0179 | AFR | YRI | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | LWK | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | LWK | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | LWK | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | YRI | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | YRI | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | ASW | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | ASW | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0045 | EUR | TSI | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0054 | EUR | TSI | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0069 | EUR | TSI | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0124 | EUR | TSI | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | GIH | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | GIH | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0191 | AFR | ACB | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | MSL | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | MSL | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | USA | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | USA | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0088 | AFR | USA | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | USA | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0067 | REF | REF | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0001 | REF | REF | PHAF1_chr16_67104941_67153544 | PHAF1 | chr16 | 67104941 | 67153544 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:67110204 | G | A | 1 | a0003 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.29G>A | p.Arg10His | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/16 | 264/2917 | 29/1269 | 10/422 | chr16 | 67110204 | |||
| chr16:67110212 | G | A | 1 | a0002 | 2 | HG01099.hp1 HG03239.hp1 |
missense_variant | MODERATE | c.37G>A | p.Gly13Arg | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/16 | 272/2917 | 37/1269 | 13/422 | chr16 | 67110212 | |||
| chr16:67145591 | C | G | 1 | a0004 | 1 | HG03491.hp2 | missense_variant | MODERATE | c.1072C>G | p.Leu358Val | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 14/16 | 1307/2917 | 1072/1269 | 358/422 | chr16 | 67145591 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:67147318 | C | G | 1 | a0001c0001t0006 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*187C>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 16/16 | 187 | chr16 | 67147318 | ||||||
| chr16:67147900 | G | A | 1 | a0001c0001t0004 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*769G>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 16/16 | 769 | chr16 | 67147900 | ||||||
| chr16:67147922 | C | A | 1 | a0001c0001t0003 | 11 | HG01884.hp1 HG02486.hp1 HG02622.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*791C>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 16/16 | 791 | chr16 | 67147922 | ||||||
| chr16:67148073 | C | G | 1 | a0001c0001t0005 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*942C>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 16/16 | 942 | chr16 | 67148073 | ||||||
| chr16:67148096 | A | G | 8 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(5): Show |
168 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*965A>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 16/16 | 965 | chr16 | 67148096 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:67110392 | C | T | 11 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(8): Show |
11 | HG00140.hp1 HG01109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.64+153C>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67110392 | |||||||
| chr16:67110464 | A | G | 89 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(86): Show |
95 | HG00140.hp1 HG00438.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.64+225A>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67110464 | |||||||
| chr16:67110506 | G | A | 1 | a0001c0001t0001g0012 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.64+267G>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67110506 | |||||||
| chr16:67110755 | C | T | 1 | a0001c0001t0002g0004 | 3 | HG02698.hp2 HG03834.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.64+516C>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67110755 | |||||||
| chr16:67110958 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.64+719C>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67110958 | |||||||
| chr16:67111020 | C | G | 1 | a0001c0001t0002g0125 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.64+781C>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67111020 | |||||||
| chr16:67111056 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.64+817C>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67111056 | |||||||
| chr16:67111072 | C | G | 9 | a0001c0001t0003g0005 a0001c0001t0003g0190 a0001c0001t0003g0191 others(6): Show |
11 | HG01884.hp1 HG02486.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.64+833C>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67111072 | |||||||
| chr16:67111606 | G | T | 20 | a0001c0001t0001g0011 a0001c0001t0001g0172 a0001c0001t0001g0173 others(17): Show |
21 | HG00609.hp2 HG00738.hp1 HG02074.hp2 others(18): Show |
intron_variant | MODIFIER | c.64+1367G>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67111606 | |||||||
| chr16:67111768 | C | T | 1 | a0001c0001t0002g0123 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.64+1529C>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67111768 | |||||||
| chr16:67112113 | T | A | 1 | a0001c0001t0001g0172 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.64+1874T>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67112113 | |||||||
| chr16:67112381 | C | CA | 14 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(11): Show |
14 | HG01361.hp1 HG01515.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.64+2164dupA | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 67112381 | ||||||
| chr16:67112799 | G | C | 92 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(89): Show |
98 | HG00140.hp1 HG00438.hp1 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.64+2560G>C | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67112799 | |||||||
| chr16:67112873 | T | C | 1 | a0001c0001t0003g0191 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.64+2634T>C | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67112873 | |||||||
| chr16:67112926 | C | G | 1 | a0001c0001t0001g0122 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.64+2687C>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67112926 | |||||||
| chr16:67113107 | G | A | 7 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0133 others(4): Show |
7 | HG01993.hp2 HG02071.hp1 HG03688.hp2 others(4): Show |
intron_variant | MODIFIER | c.64+2868G>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67113107 | |||||||
| chr16:67113320 | C | T | 1 | a0001c0001t0001g0137 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.64+3081C>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67113320 | |||||||
| chr16:67113335 | A | C | 89 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(86): Show |
95 | HG00140.hp1 HG00438.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.64+3096A>C | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67113335 | |||||||
| chr16:67113510 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.64+3271C>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67113510 | |||||||
| chr16:67113750 | C | CT | 21 | a0001c0001t0001g0011 a0001c0001t0001g0120 a0001c0001t0001g0121 others(18): Show |
22 | HG00609.hp2 HG00738.hp1 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.64+3527dupT | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 67113750 | ||||||
| chr16:67113788 | G | A | 11 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(8): Show |
11 | HG00140.hp1 HG01109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.64+3549G>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67113788 | |||||||
| chr16:67113858 | G | A | 1 | a0001c0001t0001g0020 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.64+3619G>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67113858 | |||||||
| chr16:67114011 | A | G | 1 | a0001c0001t0001g0019 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.64+3772A>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67114011 | |||||||
| chr16:67114129 | G | A | 3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 |
3 | HG02257.hp1 HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.64+3890G>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67114129 | |||||||
| chr16:67114347 | T | A | 12 | a0001c0001t0001g0008 a0001c0001t0001g0141 a0001c0001t0001g0142 others(9): Show |
13 | HG02109.hp1 HG02258.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.64+4108T>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67114347 | |||||||
| chr16:67114356 | A | T | 17 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0157 others(14): Show |
19 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.64+4117A>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67114356 | |||||||
| chr16:67114557 | A | AAAG | 11 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(8): Show |
11 | HG00140.hp1 HG01109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.64+4324_64+4326dup others(3): Show |
PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 67114557 | ||||||
| chr16:67114872 | A | G | 12 | a0001c0001t0001g0008 a0001c0001t0001g0141 a0001c0001t0001g0142 others(9): Show |
13 | HG02109.hp1 HG02258.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.64+4633A>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67114872 | |||||||
| chr16:67115102 | GAGA | G | 11 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(8): Show |
11 | HG00140.hp1 HG01109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.64+4866_64+4868del others(3): Show |
PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 67115102 | ||||||
| chr16:67115212 | T | C | 1 | a0001c0001t0002g0021 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.65-4900T>C | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67115212 | |||||||
| chr16:67115307 | G | T | 11 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(8): Show |
11 | HG00140.hp1 HG01109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.65-4805G>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67115307 | |||||||
| chr16:67115752 | T | C | 2 | a0001c0001t0001g0120 a0001c0001t0001g0121 |
2 | HG01433.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.65-4360T>C | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67115752 | |||||||
| chr16:67115989 | T | C | 1 | a0001c0001t0001g0128 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.65-4123T>C | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67115989 | |||||||
| chr16:67116796 | G | A | 1 | a0001c0001t0004g0022 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.65-3316G>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67116796 | |||||||
| chr16:67116857 | C | A | 12 | a0001c0001t0001g0008 a0001c0001t0001g0141 a0001c0001t0001g0142 others(9): Show |
13 | HG02109.hp1 HG02258.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.65-3255C>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67116857 | |||||||
| chr16:67116866 | A | G | 12 | a0001c0001t0001g0008 a0001c0001t0001g0141 a0001c0001t0001g0142 others(9): Show |
13 | HG02109.hp1 HG02258.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.65-3246A>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67116866 | |||||||
| chr16:67117199 | A | AT | 16 | a0001c0001t0001g0018 a0001c0001t0001g0108 a0001c0001t0001g0112 others(13): Show |
16 | HG01361.hp1 HG01361.hp2 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.65-2890dupT | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 67117199 | ||||||
| chr16:67117199 | A | ATT | 5 | a0001c0001t0001g0119 a0001c0001t0001g0131 a0001c0001t0001g0154 others(2): Show |
5 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-2891_65-2890dup others(2): Show |
PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 67117199 | ||||||
| chr16:67117199 | A | ATTT | 15 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0132 others(12): Show |
17 | HG02055.hp1 HG02280.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.65-2892_65-2890dup others(3): Show |
PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 67117199 | ||||||
| chr16:67117199 | A | ATTTTTTT | 12 | a0001c0001t0001g0008 a0001c0001t0001g0140 a0001c0001t0001g0142 others(9): Show |
13 | HG02109.hp1 HG02258.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.65-2896_65-2890dup others(7): Show |
PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 67117199 | ||||||
| chr16:67117199 | A | ATTTTTTT others(4): Show |
3 | a0001c0001t0001g0011 a0001c0001t0001g0181 a0001c0001t0001g0182 |
4 | HG02451.hp1 HG02717.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-2900_65-2890dup others(11): Show |
PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 67117199 | ||||||
| chr16:67117199 | A | ATTTTTTT others(5): Show |
5 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(2): Show |
5 | HG02080.hp1 HG02647.hp1 NA19056.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-2901_65-2890dup others(12): Show |
PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 67117199 | ||||||
| chr16:67117199 | A | ATTTTTTT others(6): Show |
2 | a0001c0001t0001g0187 a0001c0001t0001g0188 |
2 | HG00609.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.65-2902_65-2890dup others(13): Show |
PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 67117199 | ||||||
| chr16:67117199 | A | ATTTTTTT others(10): Show |
1 | a0001c0001t0001g0189 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.65-2906_65-2890dup others(17): Show |
PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 67117199 | ||||||
| chr16:67117199 | AT | A | 10 | a0001c0001t0001g0126 a0001c0001t0001g0133 a0001c0001t0001g0134 others(7): Show |
12 | HG00438.hp1 HG01993.hp2 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.65-2890delT | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 67117199 | ||||||
| chr16:67117199 | ATT | A | 10 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0202 others(7): Show |
10 | HG00140.hp1 HG01109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.65-2891_65-2890del others(2): Show |
PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 67117199 | ||||||
| chr16:67117199 | ATTT | A | 9 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(6): Show |
9 | HG00738.hp1 HG02559.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.65-2892_65-2890del others(3): Show |
PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 67117199 | ||||||
| chr16:67117222 | T | G | 11 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(8): Show |
11 | HG00140.hp1 HG01109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.65-2890T>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67117222 | |||||||
| chr16:67117291 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.65-2821C>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67117291 | |||||||
| chr16:67117310 | A | G | 9 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0133 others(6): Show |
9 | HG00438.hp1 HG01993.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.65-2802A>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67117310 | |||||||
| chr16:67117340 | C | T | 9 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0133 others(6): Show |
9 | HG00438.hp1 HG01993.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.65-2772C>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67117340 | |||||||
| chr16:67117373 | C | T | 2 | a0001c0001t0001g0105 a0001c0001t0001g0106 |
2 | NA19063.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.65-2739C>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67117373 | |||||||
| chr16:67117506 | A | G | 35 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0138 others(32): Show |
37 | HG00609.hp2 HG00738.hp1 HG02074.hp2 others(34): Show |
intron_variant | MODIFIER | c.65-2606A>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67117506 | |||||||
| chr16:67117548 | C | T | 1 | a0001c0001t0001g0122 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.65-2564C>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67117548 | |||||||
| chr16:67117550 | G | A | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG02257.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.65-2562G>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67117550 | |||||||
| chr16:67117573 | G | A | 1 | a0001c0001t0001g0183 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.65-2539G>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67117573 | |||||||
| chr16:67117766 | CA | C | 12 | a0001c0001t0001g0008 a0001c0001t0001g0141 a0001c0001t0001g0142 others(9): Show |
13 | HG02109.hp1 HG02258.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.65-2333delA | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 67117766 | ||||||
| chr16:67117809 | C | CT | 9 | a0001c0001t0001g0099 a0001c0001t0001g0127 a0001c0001t0001g0160 others(6): Show |
9 | HG01099.hp1 HG01192.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.65-2288dupT | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 67117809 | ||||||
| chr16:67117862 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG01192.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.65-2250G>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67117862 | |||||||
| chr16:67117884 | G | A | 2 | a0001c0001t0001g0132 a0001c0001t0001g0156 |
2 | HG02055.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.65-2228G>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67117884 | |||||||
| chr16:67117955 | A | AT | 60 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(57): Show |
64 | HG00609.hp2 HG00738.hp1 HG00741.hp1 others(61): Show |
intron_variant | MODIFIER | c.65-2140dupT | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 67117955 | ||||||
| chr16:67117955 | A | ATT | 11 | a0001c0001t0001g0126 a0001c0001t0001g0132 a0001c0001t0001g0133 others(8): Show |
11 | HG00438.hp1 HG01993.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.65-2141_65-2140dup others(2): Show |
PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 67117955 | ||||||
| chr16:67118123 | A | AT | 8 | a0001c0001t0001g0016 a0001c0001t0001g0090 a0001c0001t0001g0092 others(5): Show |
8 | HG01109.hp1 HG01515.hp1 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.65-1965dupT | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 67118123 | ||||||
| chr16:67118123 | AT | A | 26 | a0001c0001t0001g0011 a0001c0001t0001g0027 a0001c0001t0001g0028 others(23): Show |
27 | HG00609.hp2 HG00738.hp1 HG02074.hp2 others(24): Show |
intron_variant | MODIFIER | c.65-1965delT | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 67118123 | ||||||
| chr16:67118123 | ATTTTTTT others(1): Show |
A | 12 | a0001c0001t0001g0008 a0001c0001t0001g0141 a0001c0001t0001g0142 others(9): Show |
13 | HG02109.hp1 HG02258.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.65-1972_65-1965del others(8): Show |
PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 67118123 | ||||||
| chr16:67118129 | T | TG | 3 | a0001c0001t0001g0132 a0001c0001t0001g0153 a0001c0001t0001g0171 |
3 | HG02055.hp1 HG02486.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.65-1983_65-1982ins others(1): Show |
PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67118129 | |||||||
| chr16:67118130 | T | G | 58 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0017 others(55): Show |
62 | HG00140.hp1 HG00438.hp1 HG01109.hp2 others(59): Show |
intron_variant | MODIFIER | c.65-1982T>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67118130 | |||||||
| chr16:67118131 | T | G | 21 | a0001c0001t0001g0011 a0001c0001t0001g0138 a0001c0001t0001g0140 others(18): Show |
22 | HG00609.hp2 HG00738.hp1 HG02074.hp2 others(19): Show |
intron_variant | MODIFIER | c.65-1981T>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67118131 | |||||||
| chr16:67118137 | T | G | 1 | a0001c0001t0001g0019 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.65-1975T>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67118137 | |||||||
| chr16:67118138 | T | G | 12 | a0001c0001t0001g0008 a0001c0001t0001g0141 a0001c0001t0001g0142 others(9): Show |
13 | HG02109.hp1 HG02258.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.65-1974T>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67118138 | |||||||
| chr16:67118236 | G | A | 1 | a0001c0001t0002g0029 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.65-1876G>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67118236 | |||||||
| chr16:67118331 | C | CT | 30 | a0001c0001t0001g0015 a0001c0001t0001g0085 a0001c0001t0001g0095 others(27): Show |
30 | HG00140.hp1 HG00741.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.65-1758dupT | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 67118331 | ||||||
| chr16:67118331 | CT | C | 30 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0128 others(27): Show |
32 | HG00609.hp2 HG00738.hp1 HG02074.hp2 others(29): Show |
intron_variant | MODIFIER | c.65-1758delT | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 67118331 | ||||||
| chr16:67118482 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.65-1630G>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67118482 | |||||||
| chr16:67118766 | C | CT | 13 | a0001c0001t0001g0025 a0001c0001t0001g0082 a0001c0001t0001g0084 others(10): Show |
13 | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.65-1320dupT | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 67118766 | ||||||
| chr16:67118766 | C | CTTT | 4 | a0001c0001t0001g0008 a0001c0001t0001g0141 a0001c0001t0001g0143 others(1): Show |
5 | HG02559.hp1 HG02717.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-1322_65-1320dup others(3): Show |
PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 67118766 | ||||||
| chr16:67118766 | C | CTTTT | 7 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(4): Show |
7 | HG02109.hp1 HG02280.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.65-1323_65-1320dup others(4): Show |
PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 67118766 | ||||||
| chr16:67118766 | CT | C | 54 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(51): Show |
57 | HG00438.hp1 HG00609.hp2 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.65-1320delT | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 67118766 | ||||||
| chr16:67118766 | CTTTTTTT others(2): Show |
C | 6 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(3): Show |
6 | HG02922.hp1 HG02965.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.65-1328_65-1320del others(9): Show |
PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 67118766 | ||||||
| chr16:67118829 | A | G | 1 | a0001c0001t0001g0202 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.65-1283A>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67118829 | |||||||
| chr16:67119004 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.65-1108G>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67119004 | |||||||
| chr16:67119390 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.65-722A>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67119390 | |||||||
| chr16:67119523 | T | A | 43 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0141 others(40): Show |
45 | HG00140.hp1 HG00609.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.65-589T>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67119523 | |||||||
| chr16:67119524 | T | A | 3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 |
3 | HG02257.hp1 HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.65-588T>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67119524 | |||||||
| chr16:67119645 | C | T | 5 | a0001c0001t0002g0075 a0001c0001t0002g0076 a0001c0001t0002g0077 others(2): Show |
5 | HG01099.hp2 NA18944.hp2 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-467C>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67119645 | |||||||
| chr16:67119686 | A | AT | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
41 | HG01433.hp2 HG01884.hp2 HG01934.hp1 others(38): Show |
intron_variant | MODIFIER | c.65-405dupT | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 67119686 | ||||||
| chr16:67119686 | AT | A | 5 | a0001c0001t0001g0090 a0001c0001t0002g0035 a0001c0001t0002g0080 others(2): Show |
5 | HG01517.hp2 HG02896.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-405delT | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 67119686 | ||||||
| chr16:67119713 | A | T | 1 | a0001c0001t0001g0178 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.65-399A>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67119713 | |||||||
| chr16:67119854 | A | G | 1 | a0002c0002t0001g0101 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.65-258A>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67119854 | |||||||
| chr16:67119908 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.65-204G>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 1/15 | chr16 | 67119908 | |||||||
| chr16:67120377 | G | A | 20 | a0001c0001t0001g0011 a0001c0001t0001g0172 a0001c0001t0001g0173 others(17): Show |
21 | HG00609.hp2 HG00738.hp1 HG02074.hp2 others(18): Show |
intron_variant | MODIFIER | c.147+183G>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 2/15 | chr16 | 67120377 | |||||||
| chr16:67120646 | A | C | 12 | a0001c0001t0001g0008 a0001c0001t0001g0141 a0001c0001t0001g0142 others(9): Show |
13 | HG02109.hp1 HG02258.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.147+452A>C | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 2/15 | chr16 | 67120646 | |||||||
| chr16:67120990 | A | G | 5 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0033 others(2): Show |
5 | HG02922.hp1 HG02965.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.147+796A>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 2/15 | chr16 | 67120990 | |||||||
| chr16:67121194 | C | CT | 9 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0133 others(6): Show |
9 | HG00438.hp1 HG01993.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.147+1013dupT | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 67121194 | ||||||
| chr16:67121270 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.147+1076G>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 2/15 | chr16 | 67121270 | |||||||
| chr16:67121285 | G | T | 21 | a0001c0001t0001g0008 a0001c0001t0001g0141 a0001c0001t0001g0142 others(18): Show |
24 | HG01884.hp1 HG02109.hp1 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.147+1091G>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 2/15 | chr16 | 67121285 | |||||||
| chr16:67121358 | AT | A | 58 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(55): Show |
63 | HG01361.hp1 HG01433.hp1 HG01884.hp1 others(60): Show |
intron_variant | MODIFIER | c.147+1181delT | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 67121358 | ||||||
| chr16:67121358 | ATT | A | 8 | a0001c0001t0001g0127 a0001c0001t0001g0133 a0001c0001t0001g0134 others(5): Show |
8 | HG00438.hp1 HG01993.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.147+1180_147+1181d others(4): Show |
PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 67121358 | ||||||
| chr16:67121448 | C | T | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG02257.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.147+1254C>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 2/15 | chr16 | 67121448 | |||||||
| chr16:67121503 | A | G | 2 | a0001c0001t0001g0028 a0001c0001t0001g0073 |
2 | NA18947.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.147+1309A>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 2/15 | chr16 | 67121503 | |||||||
| chr16:67121667 | G | A | 1 | a0001c0001t0003g0195 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.147+1473G>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 2/15 | chr16 | 67121667 | |||||||
| chr16:67121686 | T | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0085 |
2 | HG02056.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.147+1492T>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 2/15 | chr16 | 67121686 | |||||||
| chr16:67121860 | G | A | 3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 |
3 | HG02257.hp1 HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.147+1666G>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 2/15 | chr16 | 67121860 | |||||||
| chr16:67122049 | C | T | 20 | a0001c0001t0001g0011 a0001c0001t0001g0172 a0001c0001t0001g0173 others(17): Show |
21 | HG00609.hp2 HG00738.hp1 HG02074.hp2 others(18): Show |
intron_variant | MODIFIER | c.147+1855C>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 2/15 | chr16 | 67122049 | |||||||
| chr16:67122189 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.147+1995C>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 2/15 | chr16 | 67122189 | |||||||
| chr16:67122195 | C | T | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.147+2001C>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 2/15 | chr16 | 67122195 | |||||||
| chr16:67122329 | T | C | 1 | a0001c0001t0001g0161 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.147+2135T>C | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 2/15 | chr16 | 67122329 | |||||||
| chr16:67122468 | G | A | 2 | a0001c0001t0001g0038 a0001c0001t0001g0099 |
2 | HG02738.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.147+2274G>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 2/15 | chr16 | 67122468 | |||||||
| chr16:67122570 | C | CA | 6 | a0001c0001t0001g0039 a0001c0001t0001g0079 a0001c0001t0001g0096 others(3): Show |
6 | HG00558.hp1 HG00741.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.147+2396dupA | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 67122570 | ||||||
| chr16:67122570 | CA | C | 71 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(68): Show |
77 | HG00140.hp1 HG00609.hp2 HG00738.hp1 others(74): Show |
intron_variant | MODIFIER | c.147+2396delA | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 67122570 | ||||||
| chr16:67122570 | CAA | C | 8 | a0001c0001t0001g0126 a0001c0001t0001g0152 a0001c0001t0001g0153 others(5): Show |
8 | HG00438.hp1 HG02486.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.147+2395_147+2396d others(4): Show |
PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 67122570 | ||||||
| chr16:67122570 | CAAA | C | 9 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(6): Show |
9 | HG01361.hp1 HG01993.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.147+2394_147+2396d others(5): Show |
PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 67122570 | ||||||
| chr16:67122601 | A | C | 3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 |
3 | HG02257.hp1 HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.147+2407A>C | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 2/15 | chr16 | 67122601 | |||||||
| chr16:67123088 | C | CT | 41 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(38): Show |
44 | HG00438.hp1 HG00438.hp2 HG01358.hp1 others(41): Show |
intron_variant | MODIFIER | c.148-2855dupT | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 67123088 | ||||||
| chr16:67123414 | T | TA | 20 | a0001c0001t0001g0011 a0001c0001t0001g0172 a0001c0001t0001g0173 others(17): Show |
21 | HG00609.hp2 HG00738.hp1 HG02074.hp2 others(18): Show |
intron_variant | MODIFIER | c.148-2541dupA | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 67123414 | ||||||
| chr16:67123480 | A | G | 35 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0138 others(32): Show |
37 | HG00609.hp2 HG00738.hp1 HG02074.hp2 others(34): Show |
intron_variant | MODIFIER | c.148-2479A>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 2/15 | chr16 | 67123480 | |||||||
| chr16:67123531 | C | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0090 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.148-2428C>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 2/15 | chr16 | 67123531 | |||||||
| chr16:67123541 | C | T | 2 | a0001c0001t0002g0070 a0001c0001t0002g0071 |
2 | NA18954.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.148-2418C>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 2/15 | chr16 | 67123541 | |||||||
| chr16:67123580 | A | T | 1 | a0001c0001t0002g0116 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.148-2379A>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 2/15 | chr16 | 67123580 | |||||||
| chr16:67123719 | T | G | 20 | a0001c0001t0001g0011 a0001c0001t0001g0172 a0001c0001t0001g0173 others(17): Show |
21 | HG00609.hp2 HG00738.hp1 HG02074.hp2 others(18): Show |
intron_variant | MODIFIER | c.148-2240T>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 2/15 | chr16 | 67123719 | |||||||
| chr16:67124107 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.148-1852A>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 2/15 | chr16 | 67124107 | |||||||
| chr16:67124485 | A | G | 4 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0176 others(1): Show |
4 | HG02559.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.148-1474A>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 2/15 | chr16 | 67124485 | |||||||
| chr16:67124771 | C | T | 1 | a0001c0001t0002g0115 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.148-1188C>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 2/15 | chr16 | 67124771 | |||||||
| chr16:67124901 | CA | C | 15 | a0001c0001t0001g0176 a0001c0001t0001g0199 a0001c0001t0001g0200 others(12): Show |
15 | HG00140.hp1 HG01109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.148-1041delA | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 67124901 | ||||||
| chr16:67125088 | G | A | 2 | a0001c0001t0001g0132 a0001c0001t0001g0156 |
2 | HG02055.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.148-871G>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 2/15 | chr16 | 67125088 | |||||||
| chr16:67125467 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.148-492G>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 2/15 | chr16 | 67125467 | |||||||
| chr16:67125845 | G | C | 3 | a0001c0001t0001g0009 a0001c0001t0001g0162 a0001c0001t0001g0170 |
4 | HG02896.hp2 HG02897.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.148-114G>C | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 2/15 | chr16 | 67125845 | |||||||
| chr16:67125864 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.148-95T>C | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 2/15 | chr16 | 67125864 | |||||||
| chr16:67126081 | GGCCAGTC others(8): Show |
G | 1 | a0001c0001t0001g0168 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.231+42_231+56delCA others(13): Show |
PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 67126081 | ||||||
| chr16:67126438 | T | C | 1 | a0001c0001t0002g0040 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.231+396T>C | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 3/15 | chr16 | 67126438 | |||||||
| chr16:67126594 | G | GT | 8 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0134 others(5): Show |
8 | HG00438.hp1 HG01993.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.231+552_231+553ins others(1): Show |
PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 3/15 | chr16 | 67126594 | |||||||
| chr16:67126594 | G | T | 3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 |
3 | HG02257.hp1 HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.231+552G>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 3/15 | chr16 | 67126594 | |||||||
| chr16:67126595 | G | GT | 35 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(32): Show |
38 | HG00741.hp1 HG01433.hp1 HG01433.hp2 others(35): Show |
intron_variant | MODIFIER | c.231+570dupT | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 67126595 | ||||||
| chr16:67126595 | G | T | 13 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0133 others(10): Show |
13 | HG00438.hp1 HG01993.hp2 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.231+553G>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 3/15 | chr16 | 67126595 | |||||||
| chr16:67126746 | G | A | 1 | a0001c0001t0004g0022 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.231+704G>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 3/15 | chr16 | 67126746 | |||||||
| chr16:67126781 | G | T | 1 | a0001c0001t0002g0083 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.231+739G>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 3/15 | chr16 | 67126781 | |||||||
| chr16:67126892 | C | CT | 7 | a0001c0001t0001g0015 a0001c0001t0001g0121 a0001c0001t0001g0138 others(4): Show |
7 | HG01109.hp1 HG02257.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.231+864dupT | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 67126892 | ||||||
| chr16:67127046 | G | A | 12 | a0001c0001t0001g0008 a0001c0001t0001g0141 a0001c0001t0001g0142 others(9): Show |
13 | HG02109.hp1 HG02258.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.231+1004G>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 3/15 | chr16 | 67127046 | |||||||
| chr16:67127795 | C | CA | 12 | a0001c0001t0001g0008 a0001c0001t0001g0141 a0001c0001t0001g0142 others(9): Show |
13 | HG02109.hp1 HG02258.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.231+1765dupA | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 67127795 | ||||||
| chr16:67127911 | G | A | 1 | a0001c0001t0001g0137 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.231+1869G>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 3/15 | chr16 | 67127911 | |||||||
| chr16:67127922 | C | T | 12 | a0001c0001t0001g0008 a0001c0001t0001g0141 a0001c0001t0001g0142 others(9): Show |
13 | HG02109.hp1 HG02258.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.231+1880C>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 3/15 | chr16 | 67127922 | |||||||
| chr16:67128135 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.231+2093C>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 3/15 | chr16 | 67128135 | |||||||
| chr16:67128690 | C | G | 1 | a0001c0001t0002g0066 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.232-2596C>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 3/15 | chr16 | 67128690 | |||||||
| chr16:67128749 | A | T | 46 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(43): Show |
49 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.232-2537A>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 3/15 | chr16 | 67128749 | |||||||
| chr16:67128842 | A | G | 3 | a0001c0001t0001g0131 a0001c0001t0001g0154 a0001c0001t0001g0155 |
3 | HG01884.hp2 HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.232-2444A>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 3/15 | chr16 | 67128842 | |||||||
| chr16:67128870 | G | A | 3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 |
3 | HG02257.hp1 HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.232-2416G>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 3/15 | chr16 | 67128870 | |||||||
| chr16:67128879 | A | G | 1 | a0001c0001t0003g0192 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.232-2407A>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 3/15 | chr16 | 67128879 | |||||||
| chr16:67129418 | G | C | 1 | a0001c0001t0003g0197 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.232-1868G>C | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 3/15 | chr16 | 67129418 | |||||||
| chr16:67130139 | C | T | 17 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0157 others(14): Show |
19 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.232-1147C>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 3/15 | chr16 | 67130139 | |||||||
| chr16:67130172 | C | T | 1 | a0001c0001t0002g0051 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.232-1114C>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 3/15 | chr16 | 67130172 | |||||||
| chr16:67130173 | A | C | 1 | a0001c0001t0002g0029 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.232-1113A>C | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 3/15 | chr16 | 67130173 | |||||||
| chr16:67130269 | A | G | 32 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0138 others(29): Show |
34 | HG00609.hp2 HG00738.hp1 HG02074.hp2 others(31): Show |
intron_variant | MODIFIER | c.232-1017A>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 3/15 | chr16 | 67130269 | |||||||
| chr16:67130296 | C | G | 2 | a0001c0001t0002g0070 a0001c0001t0002g0071 |
2 | NA18954.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.232-990C>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 3/15 | chr16 | 67130296 | |||||||
| chr16:67130342 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.232-944C>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 3/15 | chr16 | 67130342 | |||||||
| chr16:67130346 | C | CT | 59 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0014 others(56): Show |
63 | HG00438.hp1 HG00738.hp2 HG01358.hp1 others(60): Show |
intron_variant | MODIFIER | c.232-920dupT | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 67130346 | ||||||
| chr16:67130346 | C | CTT | 39 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0128 others(36): Show |
41 | HG00609.hp2 HG00738.hp1 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.232-921_232-920dup others(2): Show |
PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 67130346 | ||||||
| chr16:67130346 | C | CTTT | 7 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(4): Show |
7 | HG02257.hp1 HG02559.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.232-922_232-920dup others(3): Show |
PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 67130346 | ||||||
| chr16:67130346 | CT | C | 5 | a0001c0001t0002g0004 a0001c0001t0002g0034 a0001c0001t0002g0069 others(2): Show |
7 | HG01517.hp1 HG01934.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.232-920delT | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 67130346 | ||||||
| chr16:67130524 | T | G | 1 | a0001c0001t0001g0020 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.232-762T>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 3/15 | chr16 | 67130524 | |||||||
| chr16:67130555 | G | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0027 a0001c0001t0001g0036 |
4 | HG02809.hp1 HG02818.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.232-731G>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 3/15 | chr16 | 67130555 | |||||||
| chr16:67131147 | T | A | 2 | a0002c0002t0001g0100 a0002c0002t0001g0101 |
2 | HG01099.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.232-139T>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 3/15 | chr16 | 67131147 | |||||||
| chr16:67131180 | G | GT | 92 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(89): Show |
98 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.232-86dupT | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 67131180 | ||||||
| chr16:67131180 | G | GTT | 7 | a0001c0001t0001g0065 a0001c0001t0001g0095 a0001c0001t0001g0099 others(4): Show |
7 | HG02055.hp1 HG02258.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.232-87_232-86dupTT | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 67131180 | ||||||
| chr16:67131180 | GT | G | 6 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0162 others(3): Show |
7 | HG02486.hp1 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.232-86delT | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 67131180 | ||||||
| chr16:67131180 | GTT | G | 8 | a0001c0001t0003g0005 a0001c0001t0003g0190 a0001c0001t0003g0192 others(5): Show |
10 | HG01884.hp1 HG02622.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.232-87_232-86delTT | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 67131180 | ||||||
| chr16:67131378 | C | T | 12 | a0001c0001t0001g0008 a0001c0001t0001g0141 a0001c0001t0001g0142 others(9): Show |
13 | HG02109.hp1 HG02258.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.275+49C>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 4/15 | chr16 | 67131378 | |||||||
| chr16:67131739 | A | G | 2 | a0001c0001t0001g0028 a0001c0001t0001g0073 |
2 | NA18947.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.275+410A>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 4/15 | chr16 | 67131739 | |||||||
| chr16:67131778 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.275+449G>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 4/15 | chr16 | 67131778 | |||||||
| chr16:67131796 | C | G | 1 | a0001c0001t0001g0063 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.275+467C>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 4/15 | chr16 | 67131796 | |||||||
| chr16:67132017 | C | T | 20 | a0001c0001t0001g0011 a0001c0001t0001g0172 a0001c0001t0001g0173 others(17): Show |
21 | HG00609.hp2 HG00738.hp1 HG02074.hp2 others(18): Show |
intron_variant | MODIFIER | c.276-429C>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 4/15 | chr16 | 67132017 | |||||||
| chr16:67132242 | CTG | C | 3 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0168 |
3 | HG02630.hp1 HG03041.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.276-202_276-201del others(2): Show |
PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr16 | 67132242 | ||||||
| chr16:67132267 | A | G | 1 | a0001c0001t0002g0077 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.276-179A>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 4/15 | chr16 | 67132267 | |||||||
| chr16:67132569 | C | A | 1 | a0001c0001t0001g0014 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.355+44C>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 5/15 | chr16 | 67132569 | |||||||
| chr16:67132580 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.355+55A>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 5/15 | chr16 | 67132580 | |||||||
| chr16:67133376 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.450+465C>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 6/15 | chr16 | 67133376 | |||||||
| chr16:67133501 | T | TA | 34 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(31): Show |
36 | HG01109.hp2 HG01361.hp2 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.450+611dupA | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr16 | 67133501 | ||||||
| chr16:67133512 | A | C | 1 | a0001c0001t0003g0193 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.450+601A>C | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 6/15 | chr16 | 67133512 | |||||||
| chr16:67133526 | G | C | 20 | a0001c0001t0001g0011 a0001c0001t0001g0172 a0001c0001t0001g0173 others(17): Show |
21 | HG00609.hp2 HG00738.hp1 HG02074.hp2 others(18): Show |
intron_variant | MODIFIER | c.450+615G>C | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 6/15 | chr16 | 67133526 | |||||||
| chr16:67133577 | C | T | 1 | a0001c0001t0002g0076 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.451-591C>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 6/15 | chr16 | 67133577 | |||||||
| chr16:67133614 | T | C | 46 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0138 others(43): Show |
48 | HG00140.hp1 HG00609.hp2 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.451-554T>C | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 6/15 | chr16 | 67133614 | |||||||
| chr16:67133696 | C | T | 11 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(8): Show |
11 | HG00140.hp1 HG01109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.451-472C>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 6/15 | chr16 | 67133696 | |||||||
| chr16:67133768 | A | C | 2 | a0001c0001t0001g0185 a0001c0001t0001g0188 |
2 | HG00609.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.451-400A>C | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 6/15 | chr16 | 67133768 | |||||||
| chr16:67133771 | C | T | 2 | a0001c0001t0001g0062 a0001c0001t0001g0065 |
2 | HG02738.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.451-397C>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 6/15 | chr16 | 67133771 | |||||||
| chr16:67133779 | C | CA | 6 | a0001c0001t0001g0028 a0001c0001t0001g0042 a0001c0001t0001g0126 others(3): Show |
6 | HG00140.hp2 HG02300.hp1 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.451-373dupA | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr16 | 67133779 | ||||||
| chr16:67133839 | G | A | 9 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0133 others(6): Show |
9 | HG00438.hp1 HG01993.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.451-329G>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 6/15 | chr16 | 67133839 | |||||||
| chr16:67134276 | G | A | 1 | a0001c0001t0002g0098 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.548+11G>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 7/15 | chr16 | 67134276 | |||||||
| chr16:67134630 | C | G | 1 | a0001c0001t0001g0156 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.661+163C>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 8/15 | chr16 | 67134630 | |||||||
| chr16:67134766 | T | A | 1 | a0001c0001t0001g0184 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.661+299T>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 8/15 | chr16 | 67134766 | |||||||
| chr16:67135005 | A | G | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | NA18962.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.661+538A>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 8/15 | chr16 | 67135005 | |||||||
| chr16:67135157 | C | CT | 14 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(11): Show |
14 | HG00140.hp1 HG01109.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.661+698dupT | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr16 | 67135157 | ||||||
| chr16:67135258 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.661+791C>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 8/15 | chr16 | 67135258 | |||||||
| chr16:67135469 | T | TTTTTG | 4 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(1): Show |
4 | HG03209.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.661+1024_661+1028d others(7): Show |
PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr16 | 67135469 | ||||||
| chr16:67135585 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.661+1118C>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 8/15 | chr16 | 67135585 | |||||||
| chr16:67135709 | C | T | 2 | a0001c0001t0002g0034 a0001c0001t0002g0043 |
2 | HG00140.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.661+1242C>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 8/15 | chr16 | 67135709 | |||||||
| chr16:67135795 | G | T | 1 | a0001c0001t0001g0153 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.661+1328G>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 8/15 | chr16 | 67135795 | |||||||
| chr16:67135917 | A | G | 2 | a0001c0001t0001g0059 a0001c0001t0001g0114 |
2 | NA18953.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.661+1450A>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 8/15 | chr16 | 67135917 | |||||||
| chr16:67136026 | G | A | 1 | a0001c0001t0004g0022 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.661+1559G>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 8/15 | chr16 | 67136026 | |||||||
| chr16:67136219 | G | A | 11 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(8): Show |
11 | HG00140.hp1 HG01109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.661+1752G>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 8/15 | chr16 | 67136219 | |||||||
| chr16:67136505 | C | A | 11 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(8): Show |
11 | HG00140.hp1 HG01109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.661+2038C>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 8/15 | chr16 | 67136505 | |||||||
| chr16:67136529 | G | T | 41 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(38): Show |
44 | HG00544.hp1 HG00558.hp1 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.661+2062G>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 8/15 | chr16 | 67136529 | |||||||
| chr16:67136554 | C | CT | 52 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0020 others(49): Show |
58 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.661+2114dupT | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr16 | 67136554 | ||||||
| chr16:67136554 | C | CTT | 31 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(28): Show |
33 | HG01993.hp2 HG02027.hp1 HG02071.hp1 others(30): Show |
intron_variant | MODIFIER | c.661+2113_661+2114d others(4): Show |
PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr16 | 67136554 | ||||||
| chr16:67136554 | C | CTTT | 12 | a0001c0001t0001g0008 a0001c0001t0001g0126 a0001c0001t0001g0127 others(9): Show |
13 | HG00438.hp1 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.661+2112_661+2114d others(5): Show |
PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr16 | 67136554 | ||||||
| chr16:67136554 | CT | C | 15 | a0001c0001t0001g0140 a0001c0001t0001g0172 a0001c0001t0001g0173 others(12): Show |
15 | HG00738.hp1 HG01099.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.661+2114delT | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr16 | 67136554 | ||||||
| chr16:67136554 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0207 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.661+2104_661+2114d others(13): Show |
PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr16 | 67136554 | ||||||
| chr16:67136823 | G | C | 52 | a0001c0001t0001g0011 a0001c0001t0001g0126 a0001c0001t0001g0127 others(49): Show |
55 | HG00140.hp1 HG00438.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.661+2356G>C | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 8/15 | chr16 | 67136823 | |||||||
| chr16:67136867 | G | A | 1 | a0001c0001t0002g0111 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.661+2400G>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 8/15 | chr16 | 67136867 | |||||||
| chr16:67137154 | CA | C | 6 | a0001c0001t0001g0056 a0001c0001t0001g0082 a0001c0001t0001g0183 others(3): Show |
6 | HG03491.hp1 NA18954.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.661+2702delA | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr16 | 67137154 | ||||||
| chr16:67137170 | G | A | 1 | a0001c0001t0001g0137 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.661+2703G>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 8/15 | chr16 | 67137170 | |||||||
| chr16:67137411 | T | G | 1 | a0001c0001t0001g0155 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.662-2573T>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 8/15 | chr16 | 67137411 | |||||||
| chr16:67137467 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.662-2517T>C | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 8/15 | chr16 | 67137467 | |||||||
| chr16:67137566 | G | A | 1 | a0001c0001t0001g0015 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.662-2418G>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 8/15 | chr16 | 67137566 | |||||||
| chr16:67137677 | G | GT | 11 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(8): Show |
11 | HG00140.hp1 HG01109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.662-2301dupT | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr16 | 67137677 | ||||||
| chr16:67137768 | C | T | 2 | a0001c0001t0002g0034 a0001c0001t0002g0043 |
2 | HG00140.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.662-2216C>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 8/15 | chr16 | 67137768 | |||||||
| chr16:67138000 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.662-1984G>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 8/15 | chr16 | 67138000 | |||||||
| chr16:67138334 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.662-1650G>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 8/15 | chr16 | 67138334 | |||||||
| chr16:67138347 | A | G | 1 | a0001c0001t0001g0025 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.662-1637A>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 8/15 | chr16 | 67138347 | |||||||
| chr16:67138795 | T | C | 1 | a0001c0001t0001g0031 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.662-1189T>C | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 8/15 | chr16 | 67138795 | |||||||
| chr16:67138928 | T | G | 1 | a0001c0001t0001g0057 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.662-1056T>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 8/15 | chr16 | 67138928 | |||||||
| chr16:67138959 | C | G | 1 | a0001c0001t0001g0113 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.662-1025C>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 8/15 | chr16 | 67138959 | |||||||
| chr16:67139056 | C | G | 1 | a0001c0001t0001g0166 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.662-928C>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 8/15 | chr16 | 67139056 | |||||||
| chr16:67139343 | C | CT | 38 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0001g0037 others(35): Show |
39 | HG00438.hp2 HG01081.hp1 HG01358.hp2 others(36): Show |
intron_variant | MODIFIER | c.662-616dupT | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr16 | 67139343 | ||||||
| chr16:67139343 | CT | C | 23 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0018 others(20): Show |
24 | HG00609.hp2 HG00673.hp1 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.662-616delT | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr16 | 67139343 | ||||||
| chr16:67139521 | G | A | 3 | a0001c0001t0001g0142 a0001c0001t0001g0146 a0001c0001t0001g0147 |
3 | HG02109.hp1 HG02258.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.662-463G>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 8/15 | chr16 | 67139521 | |||||||
| chr16:67139539 | G | A | 1 | a0001c0001t0002g0081 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.662-445G>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 8/15 | chr16 | 67139539 | |||||||
| chr16:67139595 | C | T | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.662-389C>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 8/15 | chr16 | 67139595 | |||||||
| chr16:67139726 | TAGTGAAT others(5): Show |
T | 1 | a0001c0001t0001g0141 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.662-247_662-236del others(12): Show |
PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr16 | 67139726 | ||||||
| chr16:67140250 | T | C | 2 | a0001c0001t0001g0011 a0001c0001t0001g0186 |
3 | HG02451.hp1 HG02647.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.795+133T>C | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 9/15 | chr16 | 67140250 | |||||||
| chr16:67140309 | C | T | 20 | a0001c0001t0001g0011 a0001c0001t0001g0172 a0001c0001t0001g0173 others(17): Show |
21 | HG00609.hp2 HG00738.hp1 HG02074.hp2 others(18): Show |
intron_variant | MODIFIER | c.795+192C>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 9/15 | chr16 | 67140309 | |||||||
| chr16:67140379 | C | G | 1 | a0001c0001t0002g0115 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.796-132C>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 9/15 | chr16 | 67140379 | |||||||
| chr16:67140458 | C | T | 12 | a0001c0001t0001g0008 a0001c0001t0001g0141 a0001c0001t0001g0142 others(9): Show |
13 | HG02109.hp1 HG02258.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.796-53C>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 9/15 | chr16 | 67140458 | |||||||
| chr16:67140459 | A | G | 46 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0138 others(43): Show |
48 | HG00140.hp1 HG00609.hp2 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.796-52A>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 9/15 | chr16 | 67140459 | |||||||
| chr16:67140697 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.879+103T>C | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 10/15 | chr16 | 67140697 | |||||||
| chr16:67140771 | C | T | 2 | a0001c0001t0001g0108 a0001c0001t0001g0119 |
2 | HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.879+177C>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 10/15 | chr16 | 67140771 | |||||||
| chr16:67140970 | G | A | 2 | a0001c0001t0002g0081 a0001c0001t0002g0083 |
2 | HG00639.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.879+376G>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 10/15 | chr16 | 67140970 | |||||||
| chr16:67141238 | G | C | 1 | a0001c0001t0006g0180 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.879+644G>C | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 10/15 | chr16 | 67141238 | |||||||
| chr16:67141520 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.879+926G>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 10/15 | chr16 | 67141520 | |||||||
| chr16:67141729 | G | A | 9 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0133 others(6): Show |
9 | HG00438.hp1 HG01993.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.879+1135G>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 10/15 | chr16 | 67141729 | |||||||
| chr16:67141769 | C | T | 1 | a0001c0001t0002g0098 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.879+1175C>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 10/15 | chr16 | 67141769 | |||||||
| chr16:67141853 | G | C | 1 | a0001c0001t0001g0108 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.879+1259G>C | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 10/15 | chr16 | 67141853 | |||||||
| chr16:67141921 | GCATTTCA others(33): Show |
G | 1 | a0001c0001t0001g0130 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.879+1332_879+1371d others(42): Show |
PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr16 | 67141921 | ||||||
| chr16:67142245 | C | G | 1 | a0001c0001t0001g0209 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.879+1651C>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 10/15 | chr16 | 67142245 | |||||||
| chr16:67142566 | A | C | 1 | a0001c0001t0002g0051 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.880-1728A>C | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 10/15 | chr16 | 67142566 | |||||||
| chr16:67142891 | T | C | 36 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0138 others(33): Show |
38 | HG00609.hp2 HG00738.hp1 HG02074.hp2 others(35): Show |
intron_variant | MODIFIER | c.880-1403T>C | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 10/15 | chr16 | 67142891 | |||||||
| chr16:67143060 | G | A | 8 | a0001c0001t0003g0005 a0001c0001t0003g0190 a0001c0001t0003g0191 others(5): Show |
10 | HG01884.hp1 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.880-1234G>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 10/15 | chr16 | 67143060 | |||||||
| chr16:67143395 | G | A | 6 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(3): Show |
6 | HG02922.hp1 HG02965.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.880-899G>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 10/15 | chr16 | 67143395 | |||||||
| chr16:67143572 | C | T | 1 | a0001c0001t0002g0104 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.880-722C>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 10/15 | chr16 | 67143572 | |||||||
| chr16:67143797 | T | G | 20 | a0001c0001t0001g0011 a0001c0001t0001g0172 a0001c0001t0001g0173 others(17): Show |
21 | HG00609.hp2 HG00738.hp1 HG02074.hp2 others(18): Show |
intron_variant | MODIFIER | c.880-497T>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 10/15 | chr16 | 67143797 | |||||||
| chr16:67143843 | C | A | 1 | a0001c0001t0001g0065 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.880-451C>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 10/15 | chr16 | 67143843 | |||||||
| chr16:67143944 | A | T | 1 | a0001c0001t0001g0019 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.880-350A>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 10/15 | chr16 | 67143944 | |||||||
| chr16:67143994 | C | T | 1 | a0001c0001t0002g0046 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.880-300C>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 10/15 | chr16 | 67143994 | |||||||
| chr16:67144180 | AG | A | 22 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0131 others(19): Show |
24 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.880-112delG | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr16 | 67144180 | ||||||
| chr16:67144499 | G | C | 1 | a0001c0001t0001g0153 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.962+123G>C | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 11/15 | chr16 | 67144499 | |||||||
| chr16:67144650 | A | G | 34 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(31): Show |
37 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.963-184A>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 11/15 | chr16 | 67144650 | |||||||
| chr16:67144692 | C | G | 1 | a0001c0001t0001g0073 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.963-142C>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 11/15 | chr16 | 67144692 | |||||||
| chr16:67145070 | C | T | 97 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(94): Show |
103 | HG00140.hp1 HG00438.hp1 HG00609.hp2 others(100): Show |
intron_variant | MODIFIER | c.1006+193C>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 12/15 | chr16 | 67145070 | |||||||
| chr16:67145118 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1006+241T>C | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 12/15 | chr16 | 67145118 | |||||||
| chr16:67145308 | T | C | 3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 |
3 | HG02257.hp1 HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1007-68T>C | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 12/15 | chr16 | 67145308 | |||||||
| chr16:67145436 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1050+17C>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 13/15 | chr16 | 67145436 | |||||||
| chr16:67145497 | C | G | 1 | a0001c0001t0002g0077 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1051-73C>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 13/15 | chr16 | 67145497 | |||||||
| chr16:67145881 | C | T | 3 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0095 |
3 | HG01081.hp1 HG02258.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1109+253C>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 14/15 | chr16 | 67145881 | |||||||
| chr16:67146151 | A | G | 1 | a0001c0001t0002g0117 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1110-127A>G | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 14/15 | chr16 | 67146151 | |||||||
| chr16:67146210 | G | C | 49 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0015 others(46): Show |
51 | HG00140.hp1 HG00609.hp2 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.1110-68G>C | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 14/15 | chr16 | 67146210 | |||||||
| chr16:67146268 | T | C | 96 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(93): Show |
102 | HG00140.hp1 HG00438.hp1 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.1110-10T>C | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 14/15 | chr16 | 67146268 | |||||||
| chr16:67146272 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG02647.hp1 | splice_region_variant&intron_variant | LOW | c.1110-6C>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 14/15 | chr16 | 67146272 | |||||||
| chr16:67146601 | G | T | 1 | a0001c0001t0001g0165 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1182+251G>T | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 15/15 | chr16 | 67146601 | |||||||
| chr16:67146789 | G | A | 1 | a0001c0001t0002g0071 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1183-256G>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 15/15 | chr16 | 67146789 | |||||||
| chr16:67146852 | TG | T | 3 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0061 |
3 | HG02155.hp2 NA18962.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.1183-192delG | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 15/15 | chr16 | 67146852 | |||||||
| chr16:67146853 | G | A | 5 | a0001c0001t0001g0020 a0001c0001t0001g0068 a0001c0001t0001g0084 others(2): Show |
5 | HG00438.hp2 NA19007.hp2 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.1183-192G>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 15/15 | chr16 | 67146853 | |||||||
| chr16:67146930 | G | A | 3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 |
3 | HG02257.hp1 HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1183-115G>A | PHAF1 | ENSG00000125149.12 | transcript | ENST00000219139.8 | protein_coding | 15/15 | chr16 | 67146930 |