Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5368 |
| ensemblid | ENSG00000168081.9 |
| hgncid | 9163 |
| symbol | PNOC |
| name | prepronociceptin |
| refseq_nuc | NM_006228.5 |
| refseq_prot | NP_006219.1 |
| ensembl_nuc | ENST00000301908.8 |
| ensembl_prot | ENSP00000301908.3 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 28317268 |
| end | 28343351 |
| strand | + |
| ver | v1.2 |
| region | chr8:28317268-28343351 |
| region5000 | chr8:28312268-28348351 |
| regionname0 | PNOC_chr8_28317268_28343351 |
| regionname5000 | PNOC_chr8_28312268_28348351 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 176 | 386 | 92 | 78 | 166 | 10 | 38 | 127 | PNOC_chr8_28312268_28348351 | PNOC | MKVLL others(171): Show |
chr8 | 28312268 | 28348351 |
| a0002 | 0/0 | 176 | 34 | 0 | 0 | 30 | 0 | 4 | 29 | PNOC_chr8_28312268_28348351 | PNOC | MKVLL others(171): Show |
chr8 | 28312268 | 28348351 |
| a0003 | 0/0 | 176 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | MKVLL others(171): Show |
chr8 | 28312268 | 28348351 |
| a0004 | 0/0 | 176 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | MKVLL others(171): Show |
chr8 | 28312268 | 28348351 |
| a0005 | 0/0 | 176 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PNOC_chr8_28312268_28348351 | PNOC | MKVLL others(171): Show |
chr8 | 28312268 | 28348351 |
| a0006 | 0/0 | 176 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PNOC_chr8_28312268_28348351 | PNOC | MKVLL others(171): Show |
chr8 | 28312268 | 28348351 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 528 | 386 | 92 | 78 | 166 | 10 | 38 | PNOC_chr8_28312268_28348351 | PNOC | ATGAA others(523): Show |
chr8 | 28312268 | 28348351 | ||
| a0002c0002 | 0/0 | 528 | 34 | 0 | 0 | 30 | 0 | 4 | PNOC_chr8_28312268_28348351 | PNOC | ATGAA others(523): Show |
chr8 | 28312268 | 28348351 | ||
| a0003c0003 | 0/0 | 528 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | ATGAA others(523): Show |
chr8 | 28312268 | 28348351 | ||
| a0004c0004 | 0/0 | 528 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | ATGAA others(523): Show |
chr8 | 28312268 | 28348351 | ||
| a0005c0005 | 0/0 | 528 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | ATGAA others(523): Show |
chr8 | 28312268 | 28348351 | ||
| a0006c0006 | 0/0 | 528 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | ATGAA others(523): Show |
chr8 | 28312268 | 28348351 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1060 | 254 | 80 | 42 | 105 | 6 | 19 | PNOC_chr8_28312268_28348351 | PNOC | AACCG others(1055): Show |
chr8 | 28312268 | 28348351 |
| a0001c0001t0002 | 0/0 | 1060 | 122 | 8 | 34 | 58 | 4 | 18 | PNOC_chr8_28312268_28348351 | PNOC | AACCG others(1055): Show |
chr8 | 28312268 | 28348351 |
| a0001c0001t0003 | 0/0 | 1060 | 3 | 3 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | AACCG others(1055): Show |
chr8 | 28312268 | 28348351 |
| a0001c0001t0004 | 0/0 | 1060 | 3 | 0 | 2 | 0 | 0 | 1 | PNOC_chr8_28312268_28348351 | PNOC | AACCG others(1055): Show |
chr8 | 28312268 | 28348351 |
| a0001c0001t0005 | 0/0 | 1060 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | AACCG others(1055): Show |
chr8 | 28312268 | 28348351 |
| a0001c0001t0006 | 0/0 | 1060 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | AACCG others(1055): Show |
chr8 | 28312268 | 28348351 |
| a0001c0001t0007 | 0/0 | 1060 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | AACCG others(1055): Show |
chr8 | 28312268 | 28348351 |
| a0001c0001t0008 | 0/0 | 1060 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | AACCG others(1055): Show |
chr8 | 28312268 | 28348351 |
| a0002c0002t0001 | 0/0 | 1060 | 34 | 0 | 0 | 30 | 0 | 4 | PNOC_chr8_28312268_28348351 | PNOC | AACCG others(1055): Show |
chr8 | 28312268 | 28348351 |
| a0003c0003t0001 | 0/0 | 1060 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | AACCG others(1055): Show |
chr8 | 28312268 | 28348351 |
| a0004c0004t0003 | 0/0 | 1060 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | AACCG others(1055): Show |
chr8 | 28312268 | 28348351 |
| a0005c0005t0002 | 0/0 | 1060 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | AACCG others(1055): Show |
chr8 | 28312268 | 28348351 |
| a0006c0006t0002 | 0/0 | 1060 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | AACCG others(1055): Show |
chr8 | 28312268 | 28348351 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0003 | 0/0 | 5 | 0 | 0 | 3 | 1 | 1 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0026 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0027 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0051 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0053 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0103 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0005 | 0/0 | 5 | 0 | 2 | 0 | 0 | 3 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0006 | 0/0 | 5 | 2 | 0 | 0 | 1 | 2 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0009 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0010 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0011 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0003g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0004g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0005g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0006g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0007g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0001c0001t0008g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0002c0002t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0002c0002t0001g0012 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0002c0002t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0002c0002t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0002c0002t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0002c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0002c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0002c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0002c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0002c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0002c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0003c0003t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0004c0004t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0005c0005t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| a0006c0006t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0111 | EUR | GBR | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0011 | EUR | FIN | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0123 | EUR | FIN | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0078 | EUR | FIN | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | CHS | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | CHS | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | CHS | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | CHS | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0269 | EAS | CHS | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | CHS | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0134 | AMR | PUR | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | CHS | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG00733 | hp1 | a0003 | c0003 | t0001 | g0065 | AMR | PUR | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0063 | AMR | PUR | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0122 | AMR | PUR | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0114 | AMR | PUR | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0062 | AMR | PUR | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0145 | AMR | PUR | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0066 | AMR | PUR | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0302 | AMR | PUR | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0249 | AMR | PUR | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0259 | AMR | PUR | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0133 | AMR | PUR | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | CLM | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | CLM | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0109 | AMR | CLM | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01261 | hp1 | a0004 | c0004 | t0003 | g0190 | AMR | CLM | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0207 | AMR | CLM | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0163 | AMR | CLM | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0206 | AMR | CLM | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0162 | AMR | CLM | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | ACB | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0236 | AMR | PEL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0166 | AMR | PEL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0257 | AMR | PEL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0116 | AMR | PEL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0118 | AMR | PEL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | PEL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PEL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | KHV | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0169 | AFR | ACB | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | KHV | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | KHV | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | KHV | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | KHV | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | KHV | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | KHV | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0205 | AMR | PEL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CDX | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | CDX | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0314 | AFR | ACB | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0266 | AMR | PEL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0165 | AMR | PEL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0070 | AMR | PEL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | ACB | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | GWD | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0119 | SAS | PJL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0168 | SAS | PJL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0132 | AFR | GWD | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0031 | SAS | PJL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02738 | hp2 | a0001 | c0001 | t0004 | g0064 | SAS | PJL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0125 | AFR | GWD | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0318 | AFR | GWD | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | GWD | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | GWD | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | ESN | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | ESN | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ESN | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | ESN | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0188 | AFR | ESN | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ESN | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ESN | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0246 | AFR | ESN | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0293 | SAS | PJL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0252 | SAS | PJL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | MSL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | ESN | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | ESN | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | ESN | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0299 | AFR | ESN | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | MSL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | MSL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | MSL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0185 | SAS | PJL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0115 | SAS | PJL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | MSL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | MSL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG03486 | hp2 | a0001 | c0001 | t0008 | g0046 | AFR | MSL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0036 | SAS | PJL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0034 | SAS | PJL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0034 | SAS | PJL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0130 | AFR | ESN | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | MSL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0124 | SAS | PJL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0036 | SAS | STU | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0012 | SAS | STU | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | BEB | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | BEB | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | BEB | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0120 | SAS | BEB | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0277 | SAS | BEB | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0010 | SAS | STU | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | STU | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | STU | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | STU | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | STU | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | YRI | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | YRI | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | CHB | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CHB | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | YRI | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | YRI | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0261 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0272 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18948 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0312 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18973 | hp1 | a0002 | c0002 | t0001 | g0295 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0195 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0270 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0248 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18985 | hp2 | a0005 | c0005 | t0002 | g0002 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18986 | hp2 | a0006 | c0006 | t0002 | g0164 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18989 | hp1 | a0002 | c0002 | t0001 | g0049 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18993 | hp1 | a0002 | c0002 | t0001 | g0049 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0274 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0079 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18997 | hp2 | a0002 | c0002 | t0001 | g0301 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0284 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19001 | hp1 | a0001 | c0001 | t0006 | g0007 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0176 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0310 | AFR | LWK | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | LWK | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | LWK | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | LWK | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19054 | hp2 | a0002 | c0002 | t0001 | g0265 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19057 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19058 | hp2 | a0001 | c0001 | t0007 | g0020 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19066 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19079 | hp1 | a0002 | c0002 | t0001 | g0282 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19084 | hp1 | a0002 | c0002 | t0001 | g0281 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19086 | hp2 | a0002 | c0002 | t0001 | g0278 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19087 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19089 | hp2 | a0002 | c0002 | t0001 | g0273 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0271 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | YRI | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | YRI | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | ASW | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ASW | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0077 | EUR | TSI | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0203 | EUR | TSI | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0072 | EUR | TSI | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0006 | EUR | TSI | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0012 | SAS | GIH | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | GIH | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | ACB | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0189 | AFR | ACB | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | ACB | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | ACB | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | ACB | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | MSL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | MSL | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | USA | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | USA | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | LWK | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | LWK | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0103 | REF | REF | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0053 | REF | REF | PNOC_chr8_28312268_28348351 | PNOC | chr8 | 28312268 | 28348351 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:28329275 | G | A | 1 | a0003 | 1 | HG00733.hp1 | missense_variant | MODERATE | c.118G>A | p.Asp40Asn | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/4 | 190/1060 | 118/531 | 40/176 | chr8 | 28329275 | |||
| chr8:28339202 | C | G | 1 | a0006 | 1 | NA18986.hp2 | missense_variant | MODERATE | c.289C>G | p.Arg97Gly | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/4 | 361/1060 | 289/531 | 97/176 | chr8 | 28339202 | |||
| chr8:28339235 | C | A | 1 | a0004 | 1 | HG01261.hp1 | missense_variant | MODERATE | c.322C>A | p.Gln108Lys | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/4 | 394/1060 | 322/531 | 108/176 | chr8 | 28339235 | |||
| chr8:28339266 | C | G | 1 | a0002 | 34 | HG00621.hp1 HG03017.hp1 HG03017.hp2 others(31): Show |
missense_variant | MODERATE | c.353C>G | p.Ala118Gly | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/4 | 425/1060 | 353/531 | 118/176 | chr8 | 28339266 | |||
| chr8:28339428 | A | G | 1 | a0005 | 1 | NA18985.hp2 | missense_variant | MODERATE | c.515A>G | p.Gln172Arg | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/4 | 587/1060 | 515/531 | 172/176 | chr8 | 28339428 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:28339474 | G | A | 1 | a0001c0001t0005 | 1 | NA19087.hp1 | 3_prime_UTR_variant | MODIFIER | c.*30G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/4 | 30 | chr8 | 28339474 | ||||||
| chr8:28342954 | T | A | 2 | a0001c0001t0006 a0001c0001t0007 |
2 | NA19001.hp1 NA19058.hp2 |
3_prime_UTR_variant | MODIFIER | c.*60T>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 4/4 | 3510 | chr8 | 28342954 | ||||||
| chr8:28342955 | C | T | 2 | a0001c0001t0006 a0001c0001t0007 |
2 | NA19001.hp1 NA19058.hp2 |
3_prime_UTR_variant | MODIFIER | c.*61C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 4/4 | 3511 | chr8 | 28342955 | ||||||
| chr8:28342977 | C | A | 4 | a0001c0001t0002 a0001c0001t0006 a0005c0005t0002 others(1): Show |
125 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*83C>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 4/4 | 3533 | chr8 | 28342977 | ||||||
| chr8:28342996 | G | A | 1 | a0001c0001t0004 | 3 | HG00735.hp2 HG01069.hp1 HG02738.hp2 |
3_prime_UTR_variant | MODIFIER | c.*102G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 4/4 | 3552 | chr8 | 28342996 | ||||||
| chr8:28343168 | A | G | 2 | a0001c0001t0003 a0004c0004t0003 |
4 | HG01261.hp1 HG02109.hp2 HG02970.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*274A>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 4/4 | 3724 | chr8 | 28343168 | ||||||
| chr8:28343330 | C | T | 1 | a0001c0001t0008 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*436C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 4/4 | 3886 | chr8 | 28343330 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:28317369 | C | A | 236 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(233): Show |
311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.-24+53C>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28317369 | |||||||
| chr8:28317573 | G | A | 3 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 |
3 | HG01496.hp2 HG03710.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-24+257G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28317573 | |||||||
| chr8:28317673 | T | G | 1 | a0001c0001t0001g0057 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-24+357T>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28317673 | |||||||
| chr8:28317738 | C | T | 75 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0018 others(72): Show |
97 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.-24+422C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28317738 | |||||||
| chr8:28317833 | C | A | 6 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0245 others(3): Show |
7 | HG02451.hp2 HG02818.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.-24+517C>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28317833 | |||||||
| chr8:28317873 | C | A | 1 | a0001c0001t0001g0245 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-24+557C>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28317873 | |||||||
| chr8:28317891 | C | G | 3 | a0001c0001t0001g0042 a0001c0001t0001g0192 a0001c0001t0001g0193 |
4 | HG02258.hp2 HG02723.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-24+575C>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28317891 | |||||||
| chr8:28317911 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-24+595C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28317911 | |||||||
| chr8:28318324 | C | A | 1 | a0002c0002t0001g0248 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-24+1008C>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28318324 | |||||||
| chr8:28318464 | T | C | 49 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(46): Show |
60 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.-24+1148T>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28318464 | |||||||
| chr8:28318712 | C | CTG | 4 | a0001c0001t0001g0187 a0001c0001t0003g0188 a0001c0001t0003g0189 others(1): Show |
4 | HG01261.hp1 HG02109.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-24+1396_-24+1397i others(4): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28318712 | |||||||
| chr8:28318803 | G | T | 1 | a0001c0001t0001g0186 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-24+1487G>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28318803 | |||||||
| chr8:28318857 | C | G | 3 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0247 |
3 | HG02486.hp2 HG02735.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-24+1541C>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28318857 | |||||||
| chr8:28318876 | C | T | 1 | a0001c0001t0002g0185 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-24+1560C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28318876 | |||||||
| chr8:28319101 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-24+1785C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28319101 | |||||||
| chr8:28319226 | T | C | 3 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0247 |
3 | HG02486.hp2 HG02735.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-24+1910T>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28319226 | |||||||
| chr8:28319613 | T | C | 3 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0247 |
3 | HG02486.hp2 HG02735.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-24+2297T>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28319613 | |||||||
| chr8:28319625 | C | T | 1 | a0002c0002t0001g0312 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-24+2309C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28319625 | |||||||
| chr8:28319703 | C | G | 2 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
2 | HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-24+2387C>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28319703 | |||||||
| chr8:28319723 | G | A | 3 | a0001c0001t0001g0032 a0001c0001t0001g0098 a0001c0001t0001g0099 |
4 | HG02257.hp1 HG03041.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-24+2407G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28319723 | |||||||
| chr8:28319775 | C | T | 1 | a0001c0001t0001g0045 | 2 | HG01884.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.-24+2459C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28319775 | |||||||
| chr8:28319792 | G | C | 1 | a0001c0001t0001g0243 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-24+2476G>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28319792 | |||||||
| chr8:28319835 | A | G | 3 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0245 |
3 | HG02145.hp2 HG03516.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-24+2519A>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28319835 | |||||||
| chr8:28319859 | T | C | 3 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0247 |
3 | HG02486.hp2 HG02735.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-24+2543T>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28319859 | |||||||
| chr8:28319921 | A | C | 1 | a0001c0001t0001g0186 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-24+2605A>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28319921 | |||||||
| chr8:28320034 | T | C | 1 | a0001c0001t0001g0187 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-24+2718T>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28320034 | |||||||
| chr8:28320060 | T | G | 3 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 |
3 | HG00438.hp1 HG00438.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.-24+2744T>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28320060 | |||||||
| chr8:28320065 | TTTG | T | 4 | a0001c0001t0001g0042 a0001c0001t0001g0182 a0001c0001t0001g0192 others(1): Show |
5 | HG02258.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24+2752_-24+2754d others(5): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 28320065 | ||||||
| chr8:28320076 | C | G | 53 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0021 others(50): Show |
70 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.-24+2760C>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28320076 | |||||||
| chr8:28320084 | CTTTCTTT others(3): Show |
C | 4 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0238 others(1): Show |
4 | HG02109.hp1 HG02258.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-24+2772_-24+2781d others(12): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 28320084 | ||||||
| chr8:28320084 | CTTTCTTT others(8): Show |
C | 2 | a0001c0001t0001g0244 a0001c0001t0001g0247 |
2 | HG02486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-24+2772_-24+2786d others(17): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 28320084 | ||||||
| chr8:28320088 | CTTTCTT | C | 5 | a0001c0001t0001g0032 a0001c0001t0001g0098 a0001c0001t0001g0099 others(2): Show |
6 | HG02257.hp1 HG02735.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.-24+2776_-24+2781d others(8): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 28320088 | ||||||
| chr8:28320088 | CTTTCTTT others(2): Show |
C | 20 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(17): Show |
26 | HG00733.hp2 HG01261.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.-24+2776_-24+2784d others(11): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 28320088 | ||||||
| chr8:28320088 | CTTTCTTT others(3): Show |
C | 6 | a0001c0001t0001g0218 a0001c0001t0001g0315 a0001c0001t0001g0316 others(3): Show |
6 | HG02451.hp1 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-24+2776_-24+2785d others(12): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 28320088 | ||||||
| chr8:28320088 | CTTTCTTT others(8): Show |
C | 1 | a0001c0001t0001g0183 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-24+2776_-24+2790d others(17): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 28320088 | ||||||
| chr8:28320092 | C | CT | 115 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0011 others(112): Show |
146 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.-24+2805dupT | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 28320092 | ||||||
| chr8:28320092 | C | CTT | 31 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(28): Show |
33 | HG00558.hp1 HG00621.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.-24+2804_-24+2805d others(4): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 28320092 | ||||||
| chr8:28320092 | CT | C | 15 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0025 others(12): Show |
17 | HG00280.hp2 HG01168.hp1 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.-24+2805delT | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 28320092 | ||||||
| chr8:28320092 | CTT | C | 39 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0021 others(36): Show |
53 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.-24+2804_-24+2805d others(4): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 28320092 | ||||||
| chr8:28320092 | CTTTTTT | C | 10 | a0001c0001t0001g0014 a0001c0001t0001g0100 a0001c0001t0001g0101 others(7): Show |
12 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(9): Show |
intron_variant | MODIFIER | c.-24+2800_-24+2805d others(8): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 28320092 | ||||||
| chr8:28320092 | CTTTTTTT | C | 7 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0174 others(4): Show |
8 | HG02257.hp2 HG02280.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-24+2799_-24+2805d others(9): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 28320092 | ||||||
| chr8:28320092 | CTTTTTTT others(3): Show |
C | 5 | a0001c0001t0001g0058 a0001c0001t0001g0086 a0001c0001t0001g0089 others(2): Show |
5 | HG02622.hp1 HG02895.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24+2796_-24+2805d others(12): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 28320092 | ||||||
| chr8:28320092 | CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0167 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-24+2792_-24+2805d others(16): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 28320092 | ||||||
| chr8:28320096 | T | C | 1 | a0001c0001t0002g0249 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-24+2780T>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28320096 | |||||||
| chr8:28320098 | T | C | 10 | a0001c0001t0001g0016 a0001c0001t0001g0194 a0001c0001t0001g0196 others(7): Show |
14 | HG00423.hp1 HG01952.hp2 HG02129.hp2 others(11): Show |
intron_variant | MODIFIER | c.-24+2782T>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28320098 | |||||||
| chr8:28320099 | T | C | 1 | a0001c0001t0001g0202 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-24+2783T>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28320099 | |||||||
| chr8:28320102 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-24+2786T>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28320102 | |||||||
| chr8:28320106 | T | C | 1 | a0001c0001t0001g0058 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-24+2790T>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28320106 | |||||||
| chr8:28320121 | T | C | 6 | a0001c0001t0001g0018 a0001c0001t0001g0045 a0001c0001t0001g0057 others(3): Show |
9 | HG01884.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-24+2805T>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28320121 | |||||||
| chr8:28320122 | C | T | 1 | a0002c0002t0001g0248 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-24+2806C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28320122 | |||||||
| chr8:28320123 | A | C | 1 | a0002c0002t0001g0248 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-24+2807A>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28320123 | |||||||
| chr8:28320272 | A | T | 3 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0247 |
3 | HG02486.hp2 HG02735.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-24+2956A>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28320272 | |||||||
| chr8:28320326 | C | T | 3 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0247 |
3 | HG02486.hp2 HG02735.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-24+3010C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28320326 | |||||||
| chr8:28320353 | G | T | 2 | a0001c0001t0001g0244 a0001c0001t0001g0247 |
2 | HG02486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-24+3037G>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28320353 | |||||||
| chr8:28320363 | A | C | 1 | a0001c0001t0001g0243 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-24+3047A>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28320363 | |||||||
| chr8:28320375 | T | A | 1 | a0001c0001t0001g0048 | 2 | HG00642.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.-24+3059T>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28320375 | |||||||
| chr8:28320391 | T | C | 313 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(310): Show |
406 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(403): Show |
intron_variant | MODIFIER | c.-24+3075T>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28320391 | |||||||
| chr8:28320493 | A | C | 1 | a0001c0001t0001g0311 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-24+3177A>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28320493 | |||||||
| chr8:28320498 | A | G | 1 | a0001c0001t0002g0236 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-24+3182A>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28320498 | |||||||
| chr8:28320573 | G | A | 2 | a0001c0001t0001g0243 a0001c0001t0002g0105 |
2 | HG02735.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.-24+3257G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28320573 | |||||||
| chr8:28320647 | A | G | 3 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0247 |
3 | HG02486.hp2 HG02735.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-24+3331A>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28320647 | |||||||
| chr8:28320666 | C | T | 3 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0247 |
3 | HG02486.hp2 HG02735.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-24+3350C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28320666 | |||||||
| chr8:28320677 | C | T | 2 | a0001c0001t0001g0243 a0001c0001t0001g0302 |
2 | HG01099.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.-24+3361C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28320677 | |||||||
| chr8:28320711 | C | T | 4 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
4 | NA18943.hp2 NA18945.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.-24+3395C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28320711 | |||||||
| chr8:28320724 | G | A | 1 | a0001c0001t0001g0250 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-24+3408G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28320724 | |||||||
| chr8:28320759 | G | T | 3 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0247 |
3 | HG02486.hp2 HG02735.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-24+3443G>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28320759 | |||||||
| chr8:28320776 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-24+3460G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28320776 | |||||||
| chr8:28320837 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-24+3521C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28320837 | |||||||
| chr8:28320850 | C | CA | 7 | a0001c0001t0001g0048 a0001c0001t0001g0107 a0001c0001t0001g0251 others(4): Show |
8 | HG00642.hp1 HG00738.hp2 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.-24+3552dupA | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 28320850 | ||||||
| chr8:28320866 | A | G | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | HG00558.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-24+3550A>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28320866 | |||||||
| chr8:28320868 | A | G | 3 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0247 |
3 | HG02486.hp2 HG02735.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-24+3552A>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28320868 | |||||||
| chr8:28320946 | C | T | 3 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0247 |
3 | HG02486.hp2 HG02735.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-24+3630C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28320946 | |||||||
| chr8:28320968 | G | A | 3 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0247 |
3 | HG02486.hp2 HG02735.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-24+3652G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28320968 | |||||||
| chr8:28320996 | T | C | 160 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0011 others(157): Show |
209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.-24+3680T>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28320996 | |||||||
| chr8:28321049 | G | A | 3 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0247 |
3 | HG02486.hp2 HG02735.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-24+3733G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28321049 | |||||||
| chr8:28321136 | C | T | 3 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0247 |
3 | HG02486.hp2 HG02735.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-24+3820C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28321136 | |||||||
| chr8:28321158 | C | T | 1 | a0002c0002t0001g0301 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-24+3842C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28321158 | |||||||
| chr8:28321206 | A | AT | 185 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0011 others(182): Show |
244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.-24+3911dupT | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 28321206 | ||||||
| chr8:28321206 | A | ATT | 49 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0022 others(46): Show |
63 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.-24+3910_-24+3911d others(4): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 28321206 | ||||||
| chr8:28321206 | A | T | 3 | a0001c0001t0001g0244 a0001c0001t0001g0247 a0001c0001t0001g0300 |
3 | HG02486.hp2 NA19005.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-24+3890A>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28321206 | |||||||
| chr8:28321206 | AT | A | 7 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0262 others(4): Show |
7 | HG02027.hp2 HG02129.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-24+3911delT | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 28321206 | ||||||
| chr8:28321250 | G | T | 1 | a0001c0001t0001g0091 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-24+3934G>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28321250 | |||||||
| chr8:28321377 | G | A | 1 | a0001c0001t0002g0264 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-24+4061G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28321377 | |||||||
| chr8:28321429 | T | C | 1 | a0001c0001t0002g0109 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-24+4113T>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28321429 | |||||||
| chr8:28321441 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-24+4125G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28321441 | |||||||
| chr8:28321469 | C | A | 1 | a0001c0001t0001g0060 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-24+4153C>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28321469 | |||||||
| chr8:28321496 | A | G | 59 | a0001c0001t0001g0003 a0001c0001t0001g0025 a0001c0001t0001g0026 others(56): Show |
78 | HG00280.hp2 HG00408.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.-24+4180A>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28321496 | |||||||
| chr8:28321504 | C | T | 41 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0021 others(38): Show |
57 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.-24+4188C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28321504 | |||||||
| chr8:28321557 | T | C | 3 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0247 |
3 | HG02486.hp2 HG02735.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-24+4241T>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28321557 | |||||||
| chr8:28321876 | C | T | 4 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0238 others(1): Show |
4 | HG02109.hp1 HG02258.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-24+4560C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28321876 | |||||||
| chr8:28321897 | A | C | 1 | a0001c0001t0001g0243 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-24+4581A>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28321897 | |||||||
| chr8:28321956 | T | C | 3 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0247 |
3 | HG02486.hp2 HG02735.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-24+4640T>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28321956 | |||||||
| chr8:28322084 | C | A | 3 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0247 |
3 | HG02486.hp2 HG02735.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-24+4768C>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28322084 | |||||||
| chr8:28322160 | G | A | 3 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0247 |
3 | HG02486.hp2 HG02735.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-24+4844G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28322160 | |||||||
| chr8:28322172 | C | A | 2 | a0001c0001t0003g0188 a0001c0001t0003g0189 |
2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-24+4856C>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28322172 | |||||||
| chr8:28322172 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-24+4856C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28322172 | |||||||
| chr8:28322223 | T | C | 2 | a0001c0001t0003g0188 a0001c0001t0003g0189 |
2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-24+4907T>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28322223 | |||||||
| chr8:28322253 | A | C | 2 | a0001c0001t0001g0244 a0001c0001t0001g0247 |
2 | HG02486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-24+4937A>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28322253 | |||||||
| chr8:28322367 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-24+5051G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28322367 | |||||||
| chr8:28322377 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-24+5061G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28322377 | |||||||
| chr8:28322399 | T | A | 1 | a0001c0001t0001g0060 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-24+5083T>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28322399 | |||||||
| chr8:28322400 | A | T | 1 | a0001c0001t0001g0060 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-24+5084A>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28322400 | |||||||
| chr8:28322467 | G | A | 59 | a0001c0001t0001g0003 a0001c0001t0001g0025 a0001c0001t0001g0026 others(56): Show |
78 | HG00280.hp2 HG00408.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.-24+5151G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28322467 | |||||||
| chr8:28322571 | C | G | 1 | a0001c0001t0001g0218 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-24+5255C>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28322571 | |||||||
| chr8:28322632 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-24+5316G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28322632 | |||||||
| chr8:28322778 | C | T | 2 | a0001c0001t0001g0058 a0001c0001t0001g0089 |
2 | HG02622.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-24+5462C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28322778 | |||||||
| chr8:28322833 | C | T | 3 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0247 |
3 | HG02486.hp2 HG02735.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-24+5517C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28322833 | |||||||
| chr8:28322834 | G | A | 4 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0238 others(1): Show |
4 | HG02109.hp1 HG02258.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-24+5518G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28322834 | |||||||
| chr8:28323351 | G | A | 4 | a0001c0001t0001g0091 a0001c0001t0004g0062 a0001c0001t0004g0063 others(1): Show |
4 | HG00735.hp2 HG01069.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.-23-5784G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28323351 | |||||||
| chr8:28323543 | A | G | 4 | a0001c0001t0001g0042 a0001c0001t0001g0182 a0001c0001t0001g0192 others(1): Show |
5 | HG02258.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-23-5592A>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28323543 | |||||||
| chr8:28323621 | A | G | 1 | a0001c0001t0001g0218 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-23-5514A>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28323621 | |||||||
| chr8:28323658 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-23-5477G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28323658 | |||||||
| chr8:28323765 | T | A | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | NA18943.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.-23-5370T>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28323765 | |||||||
| chr8:28323807 | G | A | 2 | a0001c0001t0001g0244 a0001c0001t0001g0247 |
2 | HG02486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-23-5328G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28323807 | |||||||
| chr8:28323896 | C | T | 4 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0238 others(1): Show |
4 | HG02109.hp1 HG02258.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-23-5239C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28323896 | |||||||
| chr8:28323995 | G | C | 1 | a0001c0001t0001g0090 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-23-5140G>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28323995 | |||||||
| chr8:28324078 | C | T | 3 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0247 |
3 | HG02486.hp2 HG02735.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-23-5057C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28324078 | |||||||
| chr8:28324092 | A | T | 1 | a0002c0002t0001g0295 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-23-5043A>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28324092 | |||||||
| chr8:28324238 | C | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0093 |
4 | HG01256.hp1 HG01433.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.-23-4897C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28324238 | |||||||
| chr8:28324418 | T | C | 3 | a0001c0001t0001g0172 a0001c0001t0001g0177 a0001c0001t0002g0033 |
4 | HG00597.hp1 NA18999.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.-23-4717T>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28324418 | |||||||
| chr8:28324428 | G | A | 1 | a0002c0002t0001g0265 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-23-4707G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28324428 | |||||||
| chr8:28324704 | A | C | 1 | a0002c0002t0001g0252 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-23-4431A>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28324704 | |||||||
| chr8:28324904 | G | T | 1 | a0001c0001t0001g0313 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-23-4231G>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28324904 | |||||||
| chr8:28324932 | A | G | 1 | a0001c0001t0001g0051 | 2 | HG02145.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.-23-4203A>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28324932 | |||||||
| chr8:28324980 | C | T | 2 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
2 | HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-23-4155C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28324980 | |||||||
| chr8:28325288 | C | CT | 59 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(56): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.-23-3846dupT | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 28325288 | ||||||
| chr8:28325332 | C | T | 59 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(56): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.-23-3803C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28325332 | |||||||
| chr8:28325424 | C | T | 58 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(55): Show |
71 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.-23-3711C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28325424 | |||||||
| chr8:28325598 | G | C | 1 | a0001c0001t0001g0303 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-23-3537G>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28325598 | |||||||
| chr8:28325607 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-23-3528G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28325607 | |||||||
| chr8:28325617 | A | C | 2 | a0001c0001t0002g0165 a0001c0001t0002g0166 |
2 | HG01943.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.-23-3518A>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28325617 | |||||||
| chr8:28325630 | C | T | 1 | a0006c0006t0002g0164 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-23-3505C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28325630 | |||||||
| chr8:28325631 | G | A | 4 | a0001c0001t0001g0032 a0001c0001t0001g0098 a0001c0001t0001g0099 others(1): Show |
5 | HG02257.hp1 HG02630.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23-3504G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28325631 | |||||||
| chr8:28325651 | C | CA | 39 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(36): Show |
47 | HG00140.hp2 HG00642.hp1 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.-23-3470dupA | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 28325651 | ||||||
| chr8:28325672 | G | GA | 31 | a0001c0001t0001g0023 a0001c0001t0001g0172 a0001c0001t0002g0005 others(28): Show |
43 | HG00323.hp1 HG00423.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.-23-3449dupA | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 28325672 | ||||||
| chr8:28325686 | AG | A | 53 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(50): Show |
66 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.-23-3448delG | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28325686 | |||||||
| chr8:28325687 | G | A | 3 | a0001c0001t0001g0088 a0001c0001t0001g0092 a0001c0001t0004g0064 |
3 | HG01175.hp2 HG02738.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.-23-3448G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28325687 | |||||||
| chr8:28325702 | G | C | 59 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(56): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.-23-3433G>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28325702 | |||||||
| chr8:28325801 | T | C | 1 | a0001c0001t0002g0258 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-23-3334T>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28325801 | |||||||
| chr8:28325808 | C | G | 20 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0048 others(17): Show |
25 | HG00642.hp1 HG00733.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.-23-3327C>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28325808 | |||||||
| chr8:28325975 | G | C | 1 | a0002c0002t0001g0269 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-23-3160G>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28325975 | |||||||
| chr8:28326149 | C | A | 59 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(56): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.-23-2986C>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28326149 | |||||||
| chr8:28326167 | C | T | 2 | a0001c0001t0001g0087 a0001c0001t0001g0092 |
2 | NA18967.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.-23-2968C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28326167 | |||||||
| chr8:28326173 | G | A | 2 | a0001c0001t0001g0107 a0001c0001t0001g0218 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-23-2962G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28326173 | |||||||
| chr8:28326288 | G | A | 2 | a0001c0001t0002g0221 a0001c0001t0002g0255 |
2 | HG02056.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.-23-2847G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28326288 | |||||||
| chr8:28326309 | A | C | 59 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(56): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.-23-2826A>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28326309 | |||||||
| chr8:28326315 | G | A | 59 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(56): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.-23-2820G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28326315 | |||||||
| chr8:28326442 | C | T | 1 | a0002c0002t0001g0293 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-23-2693C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28326442 | |||||||
| chr8:28326457 | G | A | 2 | a0001c0001t0001g0067 a0001c0001t0001g0068 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-23-2678G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28326457 | |||||||
| chr8:28326516 | A | G | 1 | a0001c0001t0002g0163 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-23-2619A>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28326516 | |||||||
| chr8:28326600 | GC | G | 73 | a0001c0001t0001g0011 a0001c0001t0001g0023 a0001c0001t0001g0150 others(70): Show |
102 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.-23-2533delC | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 28326600 | ||||||
| chr8:28326601 | C | T | 1 | a0001c0001t0001g0029 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-23-2534C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28326601 | |||||||
| chr8:28326759 | C | G | 7 | a0001c0001t0001g0020 a0001c0001t0001g0217 a0001c0001t0001g0219 others(4): Show |
8 | HG02056.hp1 HG03669.hp2 NA18960.hp1 others(5): Show |
intron_variant | MODIFIER | c.-23-2376C>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28326759 | |||||||
| chr8:28326803 | T | C | 4 | a0001c0001t0001g0091 a0001c0001t0004g0062 a0001c0001t0004g0063 others(1): Show |
4 | HG00735.hp2 HG01069.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.-23-2332T>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28326803 | |||||||
| chr8:28326885 | A | C | 59 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(56): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.-23-2250A>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28326885 | |||||||
| chr8:28326915 | G | A | 98 | a0001c0001t0001g0011 a0001c0001t0001g0023 a0001c0001t0001g0045 others(95): Show |
134 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.-23-2220G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28326915 | |||||||
| chr8:28326983 | C | T | 20 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0048 others(17): Show |
25 | HG00642.hp1 HG00733.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.-23-2152C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28326983 | |||||||
| chr8:28327030 | T | A | 1 | a0001c0001t0002g0142 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-23-2105T>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28327030 | |||||||
| chr8:28327031 | C | T | 56 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(53): Show |
69 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.-23-2104C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28327031 | |||||||
| chr8:28327059 | T | G | 3 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0004g0064 |
3 | HG00735.hp2 HG01069.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.-23-2076T>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28327059 | |||||||
| chr8:28327091 | G | A | 59 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(56): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.-23-2044G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28327091 | |||||||
| chr8:28327140 | C | A | 2 | a0001c0001t0002g0038 a0001c0001t0002g0143 |
3 | NA18995.hp2 NA19011.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.-23-1995C>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28327140 | |||||||
| chr8:28327141 | G | A | 14 | a0002c0002t0001g0024 a0002c0002t0001g0049 a0002c0002t0001g0248 others(11): Show |
17 | HG00621.hp1 NA18939.hp1 NA18944.hp2 others(14): Show |
intron_variant | MODIFIER | c.-23-1994G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28327141 | |||||||
| chr8:28327248 | G | C | 60 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(57): Show |
73 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.-23-1887G>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28327248 | |||||||
| chr8:28327474 | G | A | 59 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(56): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.-23-1661G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28327474 | |||||||
| chr8:28327541 | G | A | 59 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(56): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.-23-1594G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28327541 | |||||||
| chr8:28327562 | A | T | 59 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(56): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.-23-1573A>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28327562 | |||||||
| chr8:28327565 | C | CT | 43 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(40): Show |
56 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.-23-1566dupT | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 28327565 | ||||||
| chr8:28327565 | C | CTT | 8 | a0001c0001t0001g0058 a0001c0001t0001g0085 a0001c0001t0001g0086 others(5): Show |
8 | HG01175.hp2 HG02622.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.-23-1567_-23-1566d others(4): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 28327565 | ||||||
| chr8:28327570 | C | T | 59 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(56): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.-23-1565C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28327570 | |||||||
| chr8:28327628 | G | A | 60 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(57): Show |
73 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.-23-1507G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28327628 | |||||||
| chr8:28327667 | A | G | 60 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(57): Show |
73 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.-23-1468A>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28327667 | |||||||
| chr8:28327708 | G | A | 1 | a0001c0001t0002g0266 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-23-1427G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28327708 | |||||||
| chr8:28327757 | C | T | 1 | a0001c0001t0001g0243 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-23-1378C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28327757 | |||||||
| chr8:28327806 | C | G | 59 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(56): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.-23-1329C>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28327806 | |||||||
| chr8:28327858 | T | C | 1 | a0001c0001t0002g0144 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-23-1277T>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28327858 | |||||||
| chr8:28327908 | G | A | 1 | a0001c0001t0001g0315 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-23-1227G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28327908 | |||||||
| chr8:28328020 | G | A | 59 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(56): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.-23-1115G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28328020 | |||||||
| chr8:28328059 | C | CT | 6 | a0001c0001t0001g0019 a0001c0001t0001g0215 a0001c0001t0001g0235 others(3): Show |
6 | HG00733.hp2 HG02055.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.-23-1050dupT | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 28328059 | ||||||
| chr8:28328059 | CT | C | 65 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(62): Show |
81 | HG00280.hp2 HG00408.hp2 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.-23-1050delT | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 28328059 | ||||||
| chr8:28328059 | CTT | C | 148 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(145): Show |
190 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.-23-1051_-23-1050d others(4): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 28328059 | ||||||
| chr8:28328059 | CTTT | C | 12 | a0001c0001t0001g0014 a0001c0001t0001g0043 a0001c0001t0001g0128 others(9): Show |
12 | HG01993.hp2 HG02965.hp1 HG03654.hp1 others(9): Show |
intron_variant | MODIFIER | c.-23-1052_-23-1050d others(5): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 28328059 | ||||||
| chr8:28328060 | T | TC | 6 | a0001c0001t0001g0054 a0001c0001t0001g0067 a0001c0001t0001g0068 others(3): Show |
6 | HG01496.hp2 HG02735.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.-23-1075_-23-1074i others(3): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28328060 | |||||||
| chr8:28328061 | T | C | 50 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(47): Show |
63 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.-23-1074T>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28328061 | |||||||
| chr8:28328062 | T | C | 9 | a0001c0001t0001g0054 a0001c0001t0001g0060 a0001c0001t0001g0067 others(6): Show |
9 | HG01496.hp2 HG02735.hp2 HG03491.hp1 others(6): Show |
intron_variant | MODIFIER | c.-23-1073T>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28328062 | |||||||
| chr8:28328063 | T | C | 58 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(55): Show |
74 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.-23-1072T>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28328063 | |||||||
| chr8:28328064 | T | C | 6 | a0001c0001t0001g0060 a0001c0001t0001g0083 a0001c0001t0001g0084 others(3): Show |
6 | HG01993.hp2 NA18957.hp2 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.-23-1071T>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28328064 | |||||||
| chr8:28328065 | T | C | 2 | a0001c0001t0001g0028 a0001c0001t0001g0087 |
3 | HG02155.hp1 NA18950.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.-23-1070T>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28328065 | |||||||
| chr8:28328066 | T | C | 1 | a0001c0001t0001g0083 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-23-1069T>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28328066 | |||||||
| chr8:28328510 | A | G | 56 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(53): Show |
69 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.-23-625A>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28328510 | |||||||
| chr8:28328513 | C | T | 98 | a0001c0001t0001g0011 a0001c0001t0001g0023 a0001c0001t0001g0045 others(95): Show |
134 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.-23-622C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28328513 | |||||||
| chr8:28328518 | T | C | 59 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(56): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.-23-617T>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28328518 | |||||||
| chr8:28328520 | T | TA | 59 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(56): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.-23-615_-23-614ins others(1): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28328520 | |||||||
| chr8:28328579 | T | C | 59 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(56): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.-23-556T>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28328579 | |||||||
| chr8:28328600 | A | G | 59 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(56): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.-23-535A>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28328600 | |||||||
| chr8:28328657 | A | G | 7 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0174 others(4): Show |
8 | HG02257.hp2 HG02280.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-23-478A>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28328657 | |||||||
| chr8:28328662 | A | G | 1 | a0001c0001t0001g0178 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-23-473A>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28328662 | |||||||
| chr8:28328690 | G | A | 2 | a0001c0001t0001g0244 a0001c0001t0001g0247 |
2 | HG02486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-23-445G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28328690 | |||||||
| chr8:28328779 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-23-356C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28328779 | |||||||
| chr8:28328800 | A | G | 59 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(56): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.-23-335A>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28328800 | |||||||
| chr8:28328878 | G | A | 59 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(56): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.-23-257G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28328878 | |||||||
| chr8:28328929 | A | G | 59 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(56): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.-23-206A>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28328929 | |||||||
| chr8:28328957 | A | C | 59 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(56): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.-23-178A>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28328957 | |||||||
| chr8:28329003 | A | G | 60 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(57): Show |
73 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.-23-132A>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28329003 | |||||||
| chr8:28329090 | T | C | 59 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(56): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.-23-45T>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 1/3 | chr8 | 28329090 | |||||||
| chr8:28329304 | A | G | 3 | a0001c0001t0001g0032 a0001c0001t0001g0098 a0001c0001t0001g0099 |
4 | HG02257.hp1 HG03041.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+21A>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28329304 | |||||||
| chr8:28329420 | A | G | 58 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(55): Show |
71 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.126+137A>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28329420 | |||||||
| chr8:28329455 | C | T | 98 | a0001c0001t0001g0011 a0001c0001t0001g0023 a0001c0001t0001g0045 others(95): Show |
134 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.126+172C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28329455 | |||||||
| chr8:28329607 | A | C | 59 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(56): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.126+324A>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28329607 | |||||||
| chr8:28329628 | A | T | 56 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(53): Show |
69 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.126+345A>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28329628 | |||||||
| chr8:28329848 | A | T | 3 | a0001c0001t0001g0018 a0001c0001t0001g0112 a0001c0001t0001g0204 |
5 | HG02615.hp1 HG02622.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.126+565A>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28329848 | |||||||
| chr8:28329892 | G | A | 59 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(56): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.126+609G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28329892 | |||||||
| chr8:28329919 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.126+636T>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28329919 | |||||||
| chr8:28329935 | C | T | 1 | a0001c0001t0002g0125 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.126+652C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28329935 | |||||||
| chr8:28330106 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.126+823C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28330106 | |||||||
| chr8:28330147 | C | T | 3 | a0001c0001t0001g0011 a0001c0001t0002g0011 a0001c0001t0002g0162 |
5 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.126+864C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28330147 | |||||||
| chr8:28330170 | C | T | 59 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(56): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.126+887C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28330170 | |||||||
| chr8:28330242 | C | G | 59 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(56): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.126+959C>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28330242 | |||||||
| chr8:28330243 | T | G | 59 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(56): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.126+960T>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28330243 | |||||||
| chr8:28330327 | G | A | 1 | a0001c0001t0002g0145 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.126+1044G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28330327 | |||||||
| chr8:28330330 | T | A | 2 | a0001c0001t0001g0244 a0001c0001t0001g0247 |
2 | HG02486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.126+1047T>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28330330 | |||||||
| chr8:28330362 | C | CTTTAT | 17 | a0001c0001t0001g0020 a0001c0001t0001g0046 a0001c0001t0001g0047 others(14): Show |
19 | HG00733.hp1 HG01884.hp1 HG02056.hp1 others(16): Show |
intron_variant | MODIFIER | c.126+1113_126+1117d others(7): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28330362 | ||||||
| chr8:28330362 | C | CTTTATTT others(3): Show |
1 | a0001c0001t0001g0217 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.126+1108_126+1117d others(12): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28330362 | ||||||
| chr8:28330362 | C | CTTTATTT others(8): Show |
6 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0203 others(3): Show |
6 | HG01243.hp2 HG02004.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.126+1103_126+1117d others(17): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28330362 | ||||||
| chr8:28330362 | C | CTTTATTT others(13): Show |
12 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0032 others(9): Show |
19 | HG00642.hp1 HG00738.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.126+1098_126+1117d others(22): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28330362 | ||||||
| chr8:28330362 | C | CTTTATTT others(18): Show |
2 | a0001c0001t0001g0183 a0001c0001t0001g0215 |
2 | HG00733.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.126+1093_126+1117d others(27): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28330362 | ||||||
| chr8:28330362 | C | CTTTATTT others(23): Show |
1 | a0004c0004t0003g0190 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.126+1088_126+1117d others(32): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28330362 | ||||||
| chr8:28330362 | C | CTTTATTT others(28): Show |
1 | a0001c0001t0003g0189 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.126+1083_126+1117d others(37): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28330362 | ||||||
| chr8:28330362 | C | CTTTATTT others(33): Show |
1 | a0001c0001t0003g0188 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.126+1117_126+1118i others(42): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28330362 | ||||||
| chr8:28330362 | CTTTAT | C | 1 | a0001c0001t0001g0027 | 3 | HG01975.hp1 HG01993.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.126+1113_126+1117d others(7): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28330362 | ||||||
| chr8:28330386 | A | AT | 4 | a0001c0001t0002g0160 a0001c0001t0002g0161 a0001c0001t0002g0169 others(1): Show |
4 | HG02055.hp2 HG02074.hp2 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+1107dupT | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28330386 | ||||||
| chr8:28330391 | A | AT | 62 | a0001c0001t0001g0011 a0001c0001t0001g0023 a0001c0001t0001g0111 others(59): Show |
91 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.126+1112dupT | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28330391 | ||||||
| chr8:28330391 | A | ATT | 5 | a0001c0001t0002g0041 a0001c0001t0002g0125 a0001c0001t0002g0159 others(2): Show |
6 | HG01433.hp1 HG02809.hp2 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+1111_126+1112d others(4): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28330391 | ||||||
| chr8:28330391 | A | T | 5 | a0001c0001t0002g0124 a0001c0001t0002g0160 a0001c0001t0002g0161 others(2): Show |
5 | HG02055.hp2 HG02074.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.126+1108A>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28330391 | |||||||
| chr8:28330395 | TA | T | 3 | a0001c0001t0001g0021 a0001c0001t0001g0104 a0001c0001t0001g0292 |
5 | HG02735.hp1 NA18968.hp2 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.126+1113delA | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28330395 | |||||||
| chr8:28330396 | A | AT | 25 | a0001c0001t0001g0026 a0001c0001t0001g0127 a0001c0001t0001g0136 others(22): Show |
29 | HG00735.hp1 HG00741.hp2 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.126+1129dupT | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28330396 | ||||||
| chr8:28330396 | A | ATTTTATT others(14): Show |
2 | a0001c0001t0001g0184 a0001c0001t0001g0318 |
2 | HG02818.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.126+1117_126+1118i others(23): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28330396 | ||||||
| chr8:28330396 | A | ATTTTATT others(14): Show |
1 | a0001c0001t0001g0245 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.126+1117_126+1118i others(23): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28330396 | ||||||
| chr8:28330396 | A | ATTTTATT others(17): Show |
1 | a0001c0001t0001g0086 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.126+1117_126+1118i others(26): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28330396 | ||||||
| chr8:28330396 | A | ATTTTATT others(3): Show |
4 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0238 others(1): Show |
4 | HG02109.hp1 HG02258.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+1117_126+1118i others(12): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28330396 | ||||||
| chr8:28330396 | A | ATTTTATT others(4): Show |
1 | a0001c0001t0001g0193 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.126+1117_126+1118i others(13): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28330396 | ||||||
| chr8:28330396 | A | ATTTTATT others(5): Show |
3 | a0001c0001t0001g0042 a0001c0001t0001g0182 a0001c0001t0001g0192 |
4 | HG02280.hp2 HG02723.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+1117_126+1118i others(14): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28330396 | ||||||
| chr8:28330396 | A | ATTTTATT others(7): Show |
1 | a0001c0001t0001g0187 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.126+1117_126+1118i others(16): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28330396 | ||||||
| chr8:28330396 | A | ATTTTATT others(9): Show |
1 | a0001c0001t0001g0173 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.126+1117_126+1118i others(18): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28330396 | ||||||
| chr8:28330396 | A | ATTTTATT others(12): Show |
2 | a0001c0001t0001g0080 a0001c0001t0001g0081 |
2 | HG03710.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.126+1117_126+1118i others(21): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28330396 | ||||||
| chr8:28330396 | A | ATTTTATT others(18): Show |
1 | a0001c0001t0001g0058 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.126+1117_126+1118i others(27): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28330396 | ||||||
| chr8:28330396 | A | ATTTTATT others(28): Show |
1 | a0001c0001t0001g0089 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.126+1117_126+1118i others(37): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28330396 | ||||||
| chr8:28330396 | A | ATTTTTTT others(11): Show |
1 | a0001c0001t0001g0067 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.126+1129_126+1130i others(20): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28330396 | ||||||
| chr8:28330396 | A | ATTTTTTT others(12): Show |
1 | a0001c0001t0001g0068 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.126+1129_126+1130i others(21): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28330396 | ||||||
| chr8:28330396 | A | T | 103 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0022 others(100): Show |
137 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.126+1113A>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28330396 | |||||||
| chr8:28330397 | T | TA | 3 | a0001c0001t0002g0034 a0001c0001t0002g0066 a0001c0001t0002g0163 |
4 | HG01081.hp2 HG01346.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+1114_126+1115i others(3): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28330397 | |||||||
| chr8:28330398 | T | TTTATTTT others(16): Show |
2 | a0001c0001t0001g0244 a0001c0001t0001g0247 |
2 | HG02486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.126+1117_126+1118i others(25): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28330398 | ||||||
| chr8:28330398 | T | TTTATTTT others(11): Show |
1 | a0001c0001t0001g0243 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.126+1117_126+1118i others(20): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28330398 | ||||||
| chr8:28330399 | T | A | 1 | a0001c0001t0001g0304 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.126+1116T>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28330399 | |||||||
| chr8:28330399 | T | TTATTTTA others(4): Show |
2 | a0001c0001t0001g0100 a0001c0001t0002g0129 |
2 | NA18965.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.126+1117_126+1118i others(13): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28330399 | ||||||
| chr8:28330400 | T | TA | 3 | a0001c0001t0001g0110 a0001c0001t0001g0126 a0001c0001t0002g0206 |
3 | HG00738.hp1 HG01361.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.126+1117_126+1118i others(3): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28330400 | |||||||
| chr8:28330400 | T | TATTTTA | 2 | a0001c0001t0001g0045 a0001c0001t0001g0174 |
3 | HG01884.hp2 HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.126+1117_126+1118i others(8): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28330400 | |||||||
| chr8:28330400 | T | TATTTTAT others(9): Show |
2 | a0001c0001t0001g0052 a0001c0001t0001g0305 |
3 | HG02809.hp1 HG03130.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.126+1117_126+1118i others(18): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28330400 | |||||||
| chr8:28330400 | T | TATTTTAT others(14): Show |
5 | a0001c0001t0001g0214 a0001c0001t0001g0296 a0001c0001t0001g0315 others(2): Show |
5 | HG02451.hp1 HG02886.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.126+1117_126+1118i others(23): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28330400 | |||||||
| chr8:28330400 | T | TATTTTAT others(19): Show |
2 | a0001c0001t0001g0313 a0001c0001t0003g0299 |
2 | HG03195.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.126+1117_126+1118i others(28): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28330400 | |||||||
| chr8:28330400 | T | TATTTTAT others(17): Show |
3 | a0001c0001t0001g0097 a0001c0001t0002g0070 a0001c0001t0004g0062 |
3 | HG01069.hp1 HG02300.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.126+1117_126+1118i others(26): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28330400 | |||||||
| chr8:28330400 | T | TATTTTTT others(11): Show |
7 | a0001c0001t0001g0029 a0001c0001t0001g0060 a0001c0001t0001g0071 others(4): Show |
8 | HG01109.hp2 HG01123.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.126+1117_126+1118i others(20): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28330400 | |||||||
| chr8:28330400 | T | TATTTTTT others(12): Show |
35 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(32): Show |
45 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.126+1117_126+1118i others(21): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28330400 | |||||||
| chr8:28330400 | T | TATTTTTT others(13): Show |
1 | a0001c0001t0004g0064 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.126+1117_126+1118i others(22): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28330400 | |||||||
| chr8:28330400 | T | TTTTTTTT others(12): Show |
2 | a0001c0001t0001g0022 a0001c0001t0001g0234 |
4 | HG01257.hp1 HG01258.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+1129_126+1130i others(21): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28330400 | ||||||
| chr8:28330401 | T | A | 29 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(26): Show |
34 | HG00733.hp1 HG00733.hp2 HG02055.hp1 others(31): Show |
intron_variant | MODIFIER | c.126+1118T>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28330401 | |||||||
| chr8:28330402 | T | A | 1 | a0001c0001t0001g0196 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.126+1119T>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28330402 | |||||||
| chr8:28330406 | T | A | 2 | a0001c0001t0001g0112 a0001c0001t0001g0204 |
2 | HG02622.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.126+1123T>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28330406 | |||||||
| chr8:28330418 | G | T | 59 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(56): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.126+1135G>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28330418 | |||||||
| chr8:28330434 | G | A | 2 | a0001c0001t0003g0188 a0001c0001t0003g0189 |
2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.126+1151G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28330434 | |||||||
| chr8:28330455 | C | T | 3 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0245 |
3 | HG02145.hp2 HG03516.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.126+1172C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28330455 | |||||||
| chr8:28330560 | C | CT | 26 | a0001c0001t0001g0032 a0001c0001t0001g0042 a0001c0001t0001g0044 others(23): Show |
29 | HG00558.hp1 HG01361.hp1 HG02015.hp2 others(26): Show |
intron_variant | MODIFIER | c.126+1295dupT | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28330560 | ||||||
| chr8:28330560 | C | CTTT | 8 | a0001c0001t0001g0030 a0001c0001t0001g0071 a0001c0001t0001g0076 others(5): Show |
9 | HG01069.hp1 NA18612.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.126+1293_126+1295d others(5): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28330560 | ||||||
| chr8:28330560 | C | CTTTT | 44 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(41): Show |
56 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.126+1292_126+1295d others(6): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28330560 | ||||||
| chr8:28330560 | C | CTTTTT | 7 | a0001c0001t0001g0031 a0001c0001t0001g0075 a0001c0001t0001g0081 others(4): Show |
7 | HG01123.hp1 HG01123.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.126+1291_126+1295d others(7): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28330560 | ||||||
| chr8:28330560 | CT | C | 9 | a0001c0001t0001g0020 a0001c0001t0001g0186 a0001c0001t0001g0203 others(6): Show |
10 | HG02965.hp1 HG03669.hp2 NA18522.hp1 others(7): Show |
intron_variant | MODIFIER | c.126+1295delT | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28330560 | ||||||
| chr8:28330637 | A | G | 59 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(56): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.126+1354A>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28330637 | |||||||
| chr8:28330647 | C | A | 1 | a0001c0001t0001g0306 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.126+1364C>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28330647 | |||||||
| chr8:28330672 | AT | A | 59 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(56): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.126+1392delT | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28330672 | ||||||
| chr8:28330998 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.126+1715G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28330998 | |||||||
| chr8:28331073 | A | G | 13 | a0001c0001t0001g0032 a0001c0001t0001g0042 a0001c0001t0001g0098 others(10): Show |
15 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.126+1790A>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28331073 | |||||||
| chr8:28331116 | T | C | 60 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(57): Show |
73 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.126+1833T>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28331116 | |||||||
| chr8:28331120 | C | T | 1 | a0001c0001t0002g0169 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.126+1837C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28331120 | |||||||
| chr8:28331122 | C | T | 59 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(56): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.126+1839C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28331122 | |||||||
| chr8:28331361 | A | G | 3 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0247 |
3 | HG02486.hp2 HG02735.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.126+2078A>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28331361 | |||||||
| chr8:28331510 | G | A | 59 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(56): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.126+2227G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28331510 | |||||||
| chr8:28331586 | C | T | 1 | a0001c0001t0001g0223 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.126+2303C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28331586 | |||||||
| chr8:28331751 | C | T | 4 | a0001c0001t0001g0037 a0001c0001t0001g0139 a0001c0001t0001g0140 others(1): Show |
5 | NA18979.hp1 NA18981.hp1 NA19055.hp1 others(2): Show |
intron_variant | MODIFIER | c.126+2468C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28331751 | |||||||
| chr8:28331768 | C | G | 4 | a0001c0001t0003g0188 a0001c0001t0003g0189 a0001c0001t0003g0299 others(1): Show |
4 | HG01261.hp1 HG02109.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+2485C>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28331768 | |||||||
| chr8:28331832 | C | G | 59 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(56): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.126+2549C>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28331832 | |||||||
| chr8:28331857 | T | A | 1 | a0001c0001t0001g0107 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.126+2574T>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28331857 | |||||||
| chr8:28331870 | C | T | 59 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(56): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.126+2587C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28331870 | |||||||
| chr8:28332062 | T | C | 1 | a0001c0001t0001g0243 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.126+2779T>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28332062 | |||||||
| chr8:28332381 | A | C | 1 | a0001c0001t0002g0123 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.126+3098A>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28332381 | |||||||
| chr8:28332519 | G | A | 2 | a0001c0001t0001g0072 a0001c0001t0001g0075 |
2 | HG01123.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.126+3236G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28332519 | |||||||
| chr8:28332743 | C | G | 59 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(56): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.126+3460C>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28332743 | |||||||
| chr8:28332843 | C | T | 2 | a0001c0001t0001g0200 a0001c0001t0001g0201 |
2 | NA18954.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.126+3560C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28332843 | |||||||
| chr8:28332989 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.126+3706C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28332989 | |||||||
| chr8:28333036 | T | A | 1 | a0001c0001t0002g0116 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.126+3753T>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28333036 | |||||||
| chr8:28333221 | C | T | 9 | a0001c0001t0001g0052 a0001c0001t0001g0214 a0001c0001t0001g0296 others(6): Show |
10 | HG02451.hp1 HG02809.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.126+3938C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28333221 | |||||||
| chr8:28333284 | A | T | 257 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(254): Show |
333 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.126+4001A>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28333284 | |||||||
| chr8:28333410 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.126+4127G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28333410 | |||||||
| chr8:28333470 | G | A | 2 | a0001c0001t0001g0244 a0001c0001t0001g0247 |
2 | HG02486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.126+4187G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28333470 | |||||||
| chr8:28333574 | G | A | 1 | a0001c0001t0001g0307 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.126+4291G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28333574 | |||||||
| chr8:28333590 | T | C | 59 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(56): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.126+4307T>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28333590 | |||||||
| chr8:28333789 | A | C | 80 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(77): Show |
98 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.126+4506A>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28333789 | |||||||
| chr8:28333904 | C | T | 1 | a0002c0002t0001g0272 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.126+4621C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28333904 | |||||||
| chr8:28333989 | T | C | 19 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0048 others(16): Show |
24 | HG00642.hp1 HG00733.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.126+4706T>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28333989 | |||||||
| chr8:28334049 | A | AAC | 36 | a0001c0001t0001g0043 a0001c0001t0001g0046 a0001c0001t0001g0047 others(33): Show |
39 | HG00438.hp1 HG00438.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.126+4805_126+4806d others(4): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28334049 | ||||||
| chr8:28334049 | A | AACAC | 20 | a0001c0001t0001g0139 a0001c0001t0001g0202 a0001c0001t0001g0212 others(17): Show |
20 | HG01952.hp1 HG02486.hp1 HG03017.hp2 others(17): Show |
intron_variant | MODIFIER | c.126+4803_126+4806d others(6): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28334049 | ||||||
| chr8:28334049 | A | AACACAC | 10 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0052 others(7): Show |
15 | HG00621.hp2 HG02451.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.126+4801_126+4806d others(8): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28334049 | ||||||
| chr8:28334049 | A | AACACACA others(1): Show |
3 | a0001c0001t0001g0204 a0001c0001t0001g0315 a0001c0001t0001g0316 |
3 | HG02622.hp2 HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.126+4799_126+4806d others(10): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28334049 | ||||||
| chr8:28334049 | AAC | A | 23 | a0001c0001t0001g0045 a0001c0001t0001g0050 a0001c0001t0001g0099 others(20): Show |
34 | HG00423.hp1 HG00558.hp2 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.126+4805_126+4806d others(4): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28334049 | ||||||
| chr8:28334049 | AACAC | A | 33 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0032 others(30): Show |
39 | HG00642.hp1 HG00733.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.126+4803_126+4806d others(6): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28334049 | ||||||
| chr8:28334049 | AACACACA others(1): Show |
A | 3 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0247 |
3 | HG02486.hp2 NA20300.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.126+4799_126+4806d others(10): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28334049 | ||||||
| chr8:28334049 | AACACACA others(3): Show |
A | 9 | a0001c0001t0001g0030 a0001c0001t0001g0071 a0001c0001t0001g0074 others(6): Show |
10 | HG02735.hp2 HG03516.hp2 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.126+4797_126+4806d others(12): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28334049 | ||||||
| chr8:28334049 | AACACACA others(5): Show |
A | 47 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0022 others(44): Show |
57 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.126+4795_126+4806d others(14): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28334049 | ||||||
| chr8:28334049 | AACACACA others(7): Show |
A | 5 | a0001c0001t0001g0042 a0001c0001t0001g0182 a0001c0001t0001g0183 others(2): Show |
6 | HG02145.hp2 HG02258.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.126+4793_126+4806d others(16): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28334049 | ||||||
| chr8:28334049 | AACACACA others(9): Show |
A | 5 | a0001c0001t0001g0156 a0001c0001t0002g0142 a0001c0001t0002g0166 others(2): Show |
5 | HG01943.hp1 HG01943.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.126+4791_126+4806d others(18): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28334049 | ||||||
| chr8:28334049 | AACACACA others(11): Show |
A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0093 |
4 | HG01256.hp1 HG01433.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+4789_126+4806d others(20): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28334049 | ||||||
| chr8:28334082 | A | G | 19 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0048 others(16): Show |
24 | HG00642.hp1 HG00733.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.126+4799A>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28334082 | |||||||
| chr8:28334189 | G | A | 255 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(252): Show |
329 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.127-4851G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28334189 | |||||||
| chr8:28334350 | C | T | 2 | a0001c0001t0001g0138 a0001c0001t0001g0231 |
2 | HG02071.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.127-4690C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28334350 | |||||||
| chr8:28334367 | C | T | 2 | a0001c0001t0002g0246 a0001c0001t0002g0314 |
2 | HG02280.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.127-4673C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28334367 | |||||||
| chr8:28334526 | G | T | 15 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0060 others(12): Show |
19 | HG00408.hp1 HG00639.hp1 HG02155.hp1 others(16): Show |
intron_variant | MODIFIER | c.127-4514G>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28334526 | |||||||
| chr8:28334551 | G | A | 1 | a0001c0001t0001g0127 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.127-4489G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28334551 | |||||||
| chr8:28334579 | T | G | 1 | a0001c0001t0001g0101 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.127-4461T>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28334579 | |||||||
| chr8:28334646 | C | T | 59 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(56): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.127-4394C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28334646 | |||||||
| chr8:28334774 | G | A | 56 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(53): Show |
69 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.127-4266G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28334774 | |||||||
| chr8:28334973 | T | C | 3 | a0001c0001t0001g0025 a0001c0001t0001g0279 a0001c0001t0001g0298 |
5 | HG02155.hp2 NA18966.hp1 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.127-4067T>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28334973 | |||||||
| chr8:28335118 | G | T | 1 | a0001c0001t0002g0041 | 2 | NA18998.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.127-3922G>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28335118 | |||||||
| chr8:28335253 | C | T | 2 | a0002c0002t0001g0049 a0002c0002t0001g0272 |
3 | NA18947.hp2 NA18989.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.127-3787C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28335253 | |||||||
| chr8:28335261 | C | A | 1 | a0001c0001t0001g0156 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.127-3779C>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28335261 | |||||||
| chr8:28335339 | C | T | 1 | a0001c0001t0002g0258 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.127-3701C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28335339 | |||||||
| chr8:28335496 | A | G | 8 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0002g0007 others(5): Show |
12 | HG02071.hp1 NA18965.hp2 NA18990.hp1 others(9): Show |
intron_variant | MODIFIER | c.127-3544A>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28335496 | |||||||
| chr8:28335630 | C | T | 56 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(53): Show |
69 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.127-3410C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28335630 | |||||||
| chr8:28335762 | C | G | 1 | a0001c0001t0001g0140 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.127-3278C>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28335762 | |||||||
| chr8:28335821 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.127-3219G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28335821 | |||||||
| chr8:28335917 | AG | A | 57 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(54): Show |
70 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.127-3121delG | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28335917 | ||||||
| chr8:28335919 | G | A | 2 | a0001c0001t0001g0244 a0001c0001t0001g0247 |
2 | HG02486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.127-3121G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28335919 | |||||||
| chr8:28335972 | G | A | 59 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(56): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.127-3068G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28335972 | |||||||
| chr8:28336016 | GC | G | 59 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(56): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.127-3022delC | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28336016 | ||||||
| chr8:28336136 | T | C | 59 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(56): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.127-2904T>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28336136 | |||||||
| chr8:28336230 | A | C | 5 | a0001c0001t0001g0048 a0001c0001t0001g0051 a0001c0001t0001g0267 others(2): Show |
7 | HG00642.hp1 HG00738.hp2 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-2810A>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28336230 | |||||||
| chr8:28336289 | T | C | 1 | a0001c0001t0001g0203 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.127-2751T>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28336289 | |||||||
| chr8:28336329 | G | T | 102 | a0001c0001t0001g0011 a0001c0001t0001g0023 a0001c0001t0001g0045 others(99): Show |
138 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.127-2711G>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28336329 | |||||||
| chr8:28336438 | G | A | 7 | a0001c0001t0001g0037 a0001c0001t0001g0043 a0001c0001t0001g0044 others(4): Show |
10 | HG02015.hp2 HG02027.hp1 NA18966.hp2 others(7): Show |
intron_variant | MODIFIER | c.127-2602G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28336438 | |||||||
| chr8:28336446 | G | A | 59 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(56): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.127-2594G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28336446 | |||||||
| chr8:28336513 | C | T | 59 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(56): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.127-2527C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28336513 | |||||||
| chr8:28336580 | G | A | 20 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0048 others(17): Show |
25 | HG00642.hp1 HG00733.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.127-2460G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28336580 | |||||||
| chr8:28336624 | C | T | 1 | a0001c0001t0001g0203 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.127-2416C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28336624 | |||||||
| chr8:28336879 | G | C | 59 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(56): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.127-2161G>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28336879 | |||||||
| chr8:28336936 | A | G | 20 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0048 others(17): Show |
25 | HG00642.hp1 HG00733.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.127-2104A>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28336936 | |||||||
| chr8:28336971 | A | G | 79 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(76): Show |
97 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.127-2069A>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28336971 | |||||||
| chr8:28337062 | T | A | 20 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0048 others(17): Show |
25 | HG00642.hp1 HG00733.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.127-1978T>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28337062 | |||||||
| chr8:28337080 | G | C | 63 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0016 others(60): Show |
86 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.127-1960G>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28337080 | |||||||
| chr8:28337087 | A | G | 59 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(56): Show |
72 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.127-1953A>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28337087 | |||||||
| chr8:28337100 | G | A | 2 | a0001c0001t0003g0188 a0001c0001t0003g0189 |
2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.127-1940G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28337100 | |||||||
| chr8:28337150 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.127-1890T>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28337150 | |||||||
| chr8:28337160 | C | T | 1 | a0001c0001t0001g0243 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.127-1880C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28337160 | |||||||
| chr8:28337229 | G | T | 2 | a0001c0001t0002g0206 a0001c0001t0002g0207 |
2 | HG01346.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.127-1811G>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28337229 | |||||||
| chr8:28337310 | T | TTA | 56 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(53): Show |
69 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.127-1729_127-1728i others(4): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28337310 | ||||||
| chr8:28337329 | G | A | 18 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0112 others(15): Show |
21 | HG01261.hp1 HG02109.hp2 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.127-1711G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28337329 | |||||||
| chr8:28337375 | C | T | 1 | a0001c0001t0001g0029 | 2 | HG01109.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.127-1665C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28337375 | |||||||
| chr8:28337376 | C | T | 3 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0008g0046 |
4 | HG02451.hp2 HG02818.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-1664C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28337376 | |||||||
| chr8:28337393 | A | C | 1 | a0001c0001t0001g0247 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.127-1647A>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28337393 | |||||||
| chr8:28337444 | C | A | 1 | a0001c0001t0001g0203 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.127-1596C>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28337444 | |||||||
| chr8:28337446 | G | C | 299 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(296): Show |
390 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(387): Show |
intron_variant | MODIFIER | c.127-1594G>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28337446 | |||||||
| chr8:28337500 | A | G | 2 | a0001c0001t0002g0005 a0001c0001t0002g0123 |
6 | HG00323.hp1 HG01081.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-1540A>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28337500 | |||||||
| chr8:28337581 | C | CT | 69 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(66): Show |
89 | HG00140.hp1 HG00408.hp1 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.127-1440dupT | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28337581 | ||||||
| chr8:28337581 | C | CTT | 157 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0020 others(154): Show |
208 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.127-1441_127-1440d others(4): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28337581 | ||||||
| chr8:28337581 | C | CTTT | 7 | a0001c0001t0001g0290 a0001c0001t0001g0298 a0001c0001t0002g0106 others(4): Show |
7 | HG02717.hp2 NA18977.hp2 NA18978.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-1442_127-1440d others(5): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28337581 | ||||||
| chr8:28337605 | C | T | 3 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0247 |
3 | HG02486.hp2 HG02735.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.127-1435C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28337605 | |||||||
| chr8:28337645 | C | G | 2 | a0001c0001t0003g0188 a0001c0001t0003g0189 |
2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.127-1395C>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28337645 | |||||||
| chr8:28337749 | A | AT | 121 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(118): Show |
151 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.127-1276dupT | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28337749 | ||||||
| chr8:28337842 | C | T | 3 | a0001c0001t0001g0107 a0001c0001t0001g0184 a0001c0001t0001g0245 |
3 | HG03516.hp2 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.127-1198C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28337842 | |||||||
| chr8:28337882 | C | T | 1 | a0001c0001t0002g0040 | 2 | HG02071.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.127-1158C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28337882 | |||||||
| chr8:28337887 | G | A | 4 | a0001c0001t0002g0039 a0001c0001t0002g0066 a0001c0001t0002g0145 others(1): Show |
5 | HG01070.hp1 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-1153G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28337887 | |||||||
| chr8:28338005 | A | G | 5 | a0001c0001t0002g0009 a0001c0001t0002g0109 a0001c0001t0002g0116 others(2): Show |
8 | HG00423.hp2 HG00621.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.127-1035A>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28338005 | |||||||
| chr8:28338008 | C | A | 64 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(61): Show |
80 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.127-1032C>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28338008 | |||||||
| chr8:28338090 | T | A | 2 | a0001c0001t0001g0173 a0001c0001t0001g0203 |
2 | HG02630.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.127-950T>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28338090 | |||||||
| chr8:28338093 | C | G | 61 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(58): Show |
77 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.127-947C>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28338093 | |||||||
| chr8:28338239 | C | T | 1 | a0002c0002t0001g0269 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.127-801C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28338239 | |||||||
| chr8:28338246 | G | A | 100 | a0001c0001t0001g0011 a0001c0001t0001g0023 a0001c0001t0001g0045 others(97): Show |
136 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.127-794G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28338246 | |||||||
| chr8:28338281 | C | G | 63 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(60): Show |
79 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.127-759C>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28338281 | |||||||
| chr8:28338368 | C | A | 1 | a0001c0001t0001g0318 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.127-672C>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28338368 | |||||||
| chr8:28338392 | G | A | 3 | a0001c0001t0001g0018 a0001c0001t0001g0112 a0001c0001t0001g0204 |
5 | HG02615.hp1 HG02622.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.127-648G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28338392 | |||||||
| chr8:28338414 | C | A | 20 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0048 others(17): Show |
25 | HG00642.hp1 HG00733.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.127-626C>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28338414 | |||||||
| chr8:28338515 | AC | A | 3 | a0001c0001t0001g0018 a0001c0001t0001g0112 a0001c0001t0001g0204 |
5 | HG02615.hp1 HG02622.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.127-524delC | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28338515 | |||||||
| chr8:28338795 | T | TA | 5 | a0001c0001t0001g0042 a0001c0001t0001g0182 a0001c0001t0001g0183 others(2): Show |
6 | HG02145.hp2 HG02258.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-244dupA | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | 28338795 | ||||||
| chr8:28338994 | A | G | 1 | a0001c0001t0001g0178 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.127-46A>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 2/3 | chr8 | 28338994 | |||||||
| chr8:28339747 | C | T | 1 | a0001c0001t0002g0266 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.*47+256C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/3 | chr8 | 28339747 | |||||||
| chr8:28340125 | G | A | 18 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0048 others(15): Show |
23 | HG00642.hp1 HG00733.hp1 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.*47+634G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/3 | chr8 | 28340125 | |||||||
| chr8:28340227 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.*47+736T>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/3 | chr8 | 28340227 | |||||||
| chr8:28340230 | G | C | 189 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0011 others(186): Show |
247 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.*47+739G>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/3 | chr8 | 28340230 | |||||||
| chr8:28340283 | CCT | C | 18 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0048 others(15): Show |
23 | HG00642.hp1 HG00733.hp1 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.*47+797_*47+798del others(2): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 28340283 | ||||||
| chr8:28340289 | T | C | 1 | a0001c0001t0002g0077 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.*47+798T>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/3 | chr8 | 28340289 | |||||||
| chr8:28340337 | C | T | 1 | a0001c0001t0002g0114 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.*47+846C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/3 | chr8 | 28340337 | |||||||
| chr8:28340380 | C | A | 5 | a0001c0001t0001g0018 a0001c0001t0001g0057 a0001c0001t0001g0112 others(2): Show |
7 | HG02615.hp1 HG02622.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.*47+889C>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/3 | chr8 | 28340380 | |||||||
| chr8:28340468 | A | G | 8 | a0001c0001t0001g0058 a0001c0001t0001g0086 a0001c0001t0001g0089 others(5): Show |
8 | HG00738.hp1 HG01891.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.*47+977A>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/3 | chr8 | 28340468 | |||||||
| chr8:28340562 | C | T | 1 | a0001c0001t0001g0228 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.*47+1071C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/3 | chr8 | 28340562 | |||||||
| chr8:28340615 | C | T | 1 | a0001c0001t0001g0186 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.*47+1124C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/3 | chr8 | 28340615 | |||||||
| chr8:28340642 | C | T | 192 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0011 others(189): Show |
250 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.*47+1151C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/3 | chr8 | 28340642 | |||||||
| chr8:28340661 | G | A | 3 | a0001c0001t0001g0191 a0001c0001t0001g0203 a0001c0001t0001g0238 |
3 | HG02109.hp1 HG03225.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.*47+1170G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/3 | chr8 | 28340661 | |||||||
| chr8:28340667 | G | A | 1 | a0001c0001t0002g0263 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.*47+1176G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/3 | chr8 | 28340667 | |||||||
| chr8:28340699 | G | A | 1 | a0001c0001t0002g0145 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.*47+1208G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/3 | chr8 | 28340699 | |||||||
| chr8:28340723 | G | A | 1 | a0001c0001t0001g0305 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.*47+1232G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/3 | chr8 | 28340723 | |||||||
| chr8:28341021 | C | T | 2 | a0001c0001t0002g0036 a0001c0001t0002g0133 |
3 | HG01192.hp2 HG03490.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.*47+1530C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/3 | chr8 | 28341021 | |||||||
| chr8:28341101 | G | A | 9 | a0001c0001t0001g0042 a0001c0001t0001g0180 a0001c0001t0001g0181 others(6): Show |
10 | HG02145.hp2 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.*47+1610G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/3 | chr8 | 28341101 | |||||||
| chr8:28341151 | T | C | 9 | a0001c0001t0001g0042 a0001c0001t0001g0180 a0001c0001t0001g0181 others(6): Show |
10 | HG02145.hp2 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.*47+1660T>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/3 | chr8 | 28341151 | |||||||
| chr8:28341163 | T | A | 1 | a0001c0001t0001g0107 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.*47+1672T>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/3 | chr8 | 28341163 | |||||||
| chr8:28341187 | T | C | 9 | a0001c0001t0001g0042 a0001c0001t0001g0180 a0001c0001t0001g0181 others(6): Show |
10 | HG02145.hp2 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.*47+1696T>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/3 | chr8 | 28341187 | |||||||
| chr8:28341199 | G | A | 41 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(38): Show |
59 | HG00140.hp2 HG00423.hp1 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.*47+1708G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/3 | chr8 | 28341199 | |||||||
| chr8:28341233 | G | A | 42 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(39): Show |
60 | HG00140.hp2 HG00423.hp1 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.*48-1709G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/3 | chr8 | 28341233 | |||||||
| chr8:28341300 | A | G | 1 | a0001c0001t0001g0186 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.*48-1642A>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/3 | chr8 | 28341300 | |||||||
| chr8:28341427 | G | A | 46 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(43): Show |
64 | HG00140.hp2 HG00423.hp1 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.*48-1515G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/3 | chr8 | 28341427 | |||||||
| chr8:28341530 | C | T | 47 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(44): Show |
65 | HG00140.hp2 HG00423.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.*48-1412C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/3 | chr8 | 28341530 | |||||||
| chr8:28341542 | C | T | 1 | a0001c0001t0001g0243 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.*48-1400C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/3 | chr8 | 28341542 | |||||||
| chr8:28341592 | T | A | 2 | a0001c0001t0001g0191 a0001c0001t0001g0238 |
2 | HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.*48-1350T>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/3 | chr8 | 28341592 | |||||||
| chr8:28341853 | A | G | 255 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(252): Show |
333 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.*48-1089A>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/3 | chr8 | 28341853 | |||||||
| chr8:28341868 | G | A | 2 | a0001c0001t0001g0212 a0001c0001t0001g0224 |
2 | NA18987.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.*48-1074G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/3 | chr8 | 28341868 | |||||||
| chr8:28342048 | A | T | 9 | a0001c0001t0001g0042 a0001c0001t0001g0180 a0001c0001t0001g0181 others(6): Show |
10 | HG02145.hp2 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.*48-894A>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/3 | chr8 | 28342048 | |||||||
| chr8:28342072 | C | T | 9 | a0001c0001t0001g0042 a0001c0001t0001g0180 a0001c0001t0001g0181 others(6): Show |
10 | HG02145.hp2 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.*48-870C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/3 | chr8 | 28342072 | |||||||
| chr8:28342119 | T | C | 1 | a0001c0001t0001g0071 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.*48-823T>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/3 | chr8 | 28342119 | |||||||
| chr8:28342166 | G | T | 1 | a0002c0002t0001g0278 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.*48-776G>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/3 | chr8 | 28342166 | |||||||
| chr8:28342268 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.*48-674G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/3 | chr8 | 28342268 | |||||||
| chr8:28342302 | G | A | 2 | a0002c0002t0001g0281 a0002c0002t0001g0284 |
2 | NA18999.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.*48-640G>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/3 | chr8 | 28342302 | |||||||
| chr8:28342326 | C | G | 1 | a0002c0002t0001g0278 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.*48-616C>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/3 | chr8 | 28342326 | |||||||
| chr8:28342347 | C | T | 243 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(240): Show |
319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.*48-595C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/3 | chr8 | 28342347 | |||||||
| chr8:28342354 | C | CA | 6 | a0001c0001t0001g0298 a0002c0002t0001g0252 a0002c0002t0001g0261 others(3): Show |
6 | HG03017.hp1 HG03017.hp2 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.*48-566dupA | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 28342354 | ||||||
| chr8:28342354 | CA | C | 35 | a0001c0001t0001g0008 a0001c0001t0001g0060 a0001c0001t0001g0085 others(32): Show |
38 | HG00323.hp1 HG00738.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.*48-566delA | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 28342354 | ||||||
| chr8:28342354 | CAA | C | 165 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0013 others(162): Show |
219 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.*48-567_*48-566del others(2): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 28342354 | ||||||
| chr8:28342354 | CAAA | C | 54 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(51): Show |
72 | HG00140.hp2 HG00423.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.*48-568_*48-566del others(3): Show |
PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 28342354 | ||||||
| chr8:28342380 | C | T | 4 | a0001c0001t0001g0019 a0001c0001t0001g0215 a0001c0001t0001g0216 others(1): Show |
6 | HG00733.hp2 HG02055.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.*48-562C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/3 | chr8 | 28342380 | |||||||
| chr8:28342400 | G | T | 2 | a0001c0001t0001g0222 a0001c0001t0001g0223 |
2 | NA18985.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.*48-542G>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/3 | chr8 | 28342400 | |||||||
| chr8:28342470 | G | C | 1 | a0001c0001t0001g0153 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.*48-472G>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/3 | chr8 | 28342470 | |||||||
| chr8:28342480 | T | A | 1 | a0001c0001t0001g0055 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.*48-462T>A | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/3 | chr8 | 28342480 | |||||||
| chr8:28342643 | T | G | 1 | a0001c0001t0001g0056 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.*48-299T>G | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/3 | chr8 | 28342643 | |||||||
| chr8:28342693 | T | C | 13 | a0001c0001t0001g0020 a0001c0001t0001g0113 a0001c0001t0001g0179 others(10): Show |
14 | HG00733.hp1 HG02056.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.*48-249T>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/3 | chr8 | 28342693 | |||||||
| chr8:28342694 | G | C | 13 | a0001c0001t0001g0020 a0001c0001t0001g0113 a0001c0001t0001g0179 others(10): Show |
14 | HG00733.hp1 HG02056.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.*48-248G>C | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/3 | chr8 | 28342694 | |||||||
| chr8:28342810 | C | T | 1 | a0001c0001t0001g0140 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.*48-132C>T | PNOC | ENSG00000168081.9 | transcript | ENST00000301908.8 | protein_coding | 3/3 | chr8 | 28342810 |