Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 282809 |
| ensemblid | ENSG00000139323.14 |
| hgncid | 30836 |
| symbol | POC1B |
| name | POC1 centriolar protein B |
| refseq_nuc | NM_172240.3 |
| refseq_prot | NP_758440.1 |
| ensembl_nuc | ENST00000313546.8 |
| ensembl_prot | ENSP00000323302.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 89419718 |
| end | 89526047 |
| strand | - |
| ver | v1.2 |
| region | chr12:89419718-89526047 |
| region5000 | chr12:89414718-89531047 |
| regionname0 | POC1B_chr12_89419718_89526047 |
| regionname5000 | POC1B_chr12_89414718_89531047 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 478 | 368 | 81 | 68 | 171 | 10 | 36 | 130 | POC1B_chr12_89414718_89531047 | POC1B | MASAT others(473): Show |
chr12 | 89414718 | 89531047 |
| a0002 | 0/0 | 478 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | MASAT others(473): Show |
chr12 | 89414718 | 89531047 |
| a0003 | 0/0 | 478 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | MASAT others(473): Show |
chr12 | 89414718 | 89531047 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1434 | 361 | 80 | 68 | 165 | 10 | 36 | POC1B_chr12_89414718_89531047 | POC1B | ATGGC others(1429): Show |
chr12 | 89414718 | 89531047 | ||
| a0001c0002 | 0/0 | 1434 | 5 | 0 | 0 | 5 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | ATGGC others(1429): Show |
chr12 | 89414718 | 89531047 | ||
| a0001c0004 | 0/0 | 1434 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | ATGGC others(1429): Show |
chr12 | 89414718 | 89531047 | ||
| a0001c0005 | 0/0 | 1434 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | ATGGC others(1429): Show |
chr12 | 89414718 | 89531047 | ||
| a0002c0003 | 0/0 | 1434 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | ATGGC others(1429): Show |
chr12 | 89414718 | 89531047 | ||
| a0003c0006 | 0/0 | 1434 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | ATGGC others(1429): Show |
chr12 | 89414718 | 89531047 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3024 | 281 | 58 | 61 | 125 | 10 | 25 | POC1B_chr12_89414718_89531047 | POC1B | GACTG others(3019): Show |
chr12 | 89414718 | 89531047 |
| a0001c0001t0002 | 0/0 | 3019 | 51 | 1 | 3 | 36 | 0 | 11 | POC1B_chr12_89414718_89531047 | POC1B | GACTG others(3014): Show |
chr12 | 89414718 | 89531047 |
| a0001c0001t0003 | 0/0 | 3024 | 4 | 4 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | GACTG others(3019): Show |
chr12 | 89414718 | 89531047 |
| a0001c0001t0004 | 0/0 | 3024 | 3 | 2 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | GACTG others(3019): Show |
chr12 | 89414718 | 89531047 |
| a0001c0001t0005 | 0/0 | 3024 | 3 | 3 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | GACTG others(3019): Show |
chr12 | 89414718 | 89531047 |
| a0001c0001t0006 | 0/0 | 3024 | 3 | 1 | 2 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | GACTG others(3019): Show |
chr12 | 89414718 | 89531047 |
| a0001c0001t0007 | 0/0 | 3019 | 3 | 0 | 0 | 3 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | GACTG others(3014): Show |
chr12 | 89414718 | 89531047 |
| a0001c0001t0008 | 0/0 | 3023 | 3 | 3 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | GACTG others(3018): Show |
chr12 | 89414718 | 89531047 |
| a0001c0001t0009 | 0/0 | 3024 | 2 | 2 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | GACTG others(3019): Show |
chr12 | 89414718 | 89531047 |
| a0001c0001t0010 | 0/0 | 3024 | 2 | 2 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | GACTG others(3019): Show |
chr12 | 89414718 | 89531047 |
| a0001c0001t0011 | 0/0 | 3024 | 2 | 1 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | GACTG others(3019): Show |
chr12 | 89414718 | 89531047 |
| a0001c0001t0012 | 0/0 | 3023 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | GACTG others(3018): Show |
chr12 | 89414718 | 89531047 |
| a0001c0001t0013 | 0/0 | 3010 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | GACTG others(3005): Show |
chr12 | 89414718 | 89531047 |
| a0001c0001t0014 | 0/0 | 3024 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | GACTG others(3019): Show |
chr12 | 89414718 | 89531047 |
| a0001c0001t0015 | 0/0 | 3024 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | GACTG others(3019): Show |
chr12 | 89414718 | 89531047 |
| a0001c0002t0001 | 0/0 | 3024 | 4 | 0 | 0 | 4 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | GACTG others(3019): Show |
chr12 | 89414718 | 89531047 |
| a0001c0002t0002 | 0/0 | 3019 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | GACTG others(3014): Show |
chr12 | 89414718 | 89531047 |
| a0001c0004t0001 | 0/0 | 3024 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | GACTG others(3019): Show |
chr12 | 89414718 | 89531047 |
| a0001c0005t0002 | 0/0 | 3019 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | GACTG others(3014): Show |
chr12 | 89414718 | 89531047 |
| a0002c0003t0001 | 0/0 | 3024 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | GACTG others(3019): Show |
chr12 | 89414718 | 89531047 |
| a0003c0006t0001 | 0/0 | 3024 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | GACTG others(3019): Show |
chr12 | 89414718 | 89531047 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0190 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0238 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0003g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0003g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0004g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0004g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0004g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0005g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0005g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0005g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0006g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0006g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0006g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0007g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0007g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0007g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0008g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0008g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0008g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0009g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0009g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0010g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0010g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0011g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0011g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0012g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0013g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0014g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0001t0015g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0004t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0001c0005t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0002c0003t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| a0003c0006t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0195 | EUR | GBR | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0354 | EUR | GBR | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0274 | EUR | FIN | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0338 | EUR | FIN | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | CHS | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | CHS | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | CHS | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0263 | EAS | CHS | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | CHS | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | CHS | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0262 | EAS | CHS | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0040 | AMR | PUR | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | PUR | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | CHS | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0342 | AMR | PUR | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01070 | hp2 | a0001 | c0001 | t0006 | g0227 | AMR | PUR | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0309 | AMR | PUR | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0341 | AMR | PUR | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0156 | AMR | PUR | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0328 | AMR | PUR | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0347 | AMR | PUR | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | CLM | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0303 | AMR | CLM | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01361 | hp1 | a0001 | c0001 | t0006 | g0228 | AMR | CLM | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0337 | AMR | CLM | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0339 | AMR | CLM | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0253 | EUR | IBS | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0336 | EUR | IBS | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0284 | AFR | ACB | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01891 | hp2 | a0001 | c0001 | t0006 | g0226 | AFR | ACB | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0282 | AMR | PEL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0343 | AMR | PEL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0353 | AMR | PEL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0129 | AMR | PEL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0244 | EAS | KHV | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02055 | hp2 | a0002 | c0003 | t0001 | g0288 | AFR | ACB | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | KHV | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | KHV | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0345 | EAS | KHV | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | KHV | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | KHV | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | KHV | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | KHV | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | KHV | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | KHV | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | CDX | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | CDX | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | CDX | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02165 | hp2 | a0003 | c0006 | t0001 | g0322 | EAS | CDX | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | ACB | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02258 | hp2 | a0001 | c0001 | t0010 | g0235 | AFR | ACB | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | ACB | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0205 | AFR | ACB | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0312 | AMR | PEL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02451 | hp1 | a0001 | c0001 | t0011 | g0363 | AFR | ACB | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | ACB | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | KHV | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0294 | SAS | PJL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0044 | AFR | GWD | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0302 | AFR | GWD | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02622 | hp2 | a0001 | c0001 | t0008 | g0361 | AFR | GWD | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0335 | AFR | GWD | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0287 | AFR | GWD | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02647 | hp2 | a0001 | c0001 | t0009 | g0009 | AFR | GWD | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02717 | hp2 | a0001 | c0001 | t0008 | g0359 | AFR | GWD | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0355 | SAS | PJL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0208 | SAS | PJL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02895 | hp1 | a0001 | c0001 | t0009 | g0008 | AFR | GWD | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | ESN | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0352 | AFR | ESN | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ESN | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ESN | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0344 | SAS | PJL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0042 | AFR | GWD | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | MSL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | MSL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG03130 | hp2 | a0001 | c0004 | t0001 | g0264 | AFR | ESN | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0351 | AFR | ESN | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | ESN | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG03209 | hp2 | a0001 | c0001 | t0015 | g0358 | AFR | MSL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | MSL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | MSL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0171 | SAS | PJL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0293 | SAS | PJL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG03453 | hp1 | a0001 | c0001 | t0008 | g0360 | AFR | MSL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | MSL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | MSL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | MSL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0128 | SAS | PJL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0291 | SAS | PJL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0357 | SAS | PJL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0308 | SAS | PJL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0045 | AFR | GWD | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0134 | AFR | MSL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0286 | SAS | PJL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0346 | SAS | PJL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0321 | SAS | STU | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | STU | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0135 | SAS | PJL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0169 | SAS | PJL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0058 | SAS | PJL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0307 | SAS | BEB | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0019 | SAS | BEB | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0290 | SAS | BEB | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0150 | SAS | STU | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | STU | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0306 | SAS | BEB | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0021 | SAS | BEB | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | STU | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0257 | SAS | STU | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | STU | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0299 | SAS | STU | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | CHB | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | CHB | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CHB | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | CHB | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0043 | AFR | YRI | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18951 | hp2 | a0001 | c0001 | t0014 | g0145 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18959 | hp1 | a0001 | c0001 | t0007 | g0278 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18962 | hp1 | a0001 | c0005 | t0002 | g0138 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18967 | hp2 | a0001 | c0002 | t0001 | g0267 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18982 | hp2 | a0001 | c0002 | t0002 | g0261 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18989 | hp1 | a0001 | c0001 | t0007 | g0033 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18999 | hp1 | a0001 | c0001 | t0007 | g0277 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0356 | AFR | LWK | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19043 | hp2 | a0001 | c0001 | t0010 | g0234 | AFR | LWK | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | YRI | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | YRI | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ASW | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0350 | AFR | ASW | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0289 | EUR | TSI | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0098 | EUR | TSI | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0062 | EUR | TSI | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0254 | EUR | TSI | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0119 | SAS | GIH | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | GIH | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | CLM | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG01123 | hp2 | a0001 | c0001 | t0011 | g0362 | AMR | CLM | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02486 | hp1 | a0001 | c0001 | t0012 | g0106 | AFR | ACB | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | ACB | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0331 | AFR | MSL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | MSL | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | USA | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA20300 | hp2 | a0001 | c0001 | t0013 | g0319 | AFR | USA | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | LWK | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | LWK | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0190 | REF | REF | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0238 | REF | REF | POC1B_chr12_89414718_89531047 | POC1B | chr12 | 89414718 | 89531047 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:89459666 | A | G | 1 | a0002 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.1085T>C | p.Met362Thr | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/12 | 1237/3024 | 1085/1437 | 362/478 | chr12 | 89459666 | |||
| chr12:89497325 | T | C | 1 | a0003 | 1 | HG02165.hp2 | missense_variant | MODERATE | c.118A>G | p.Thr40Ala | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 3/12 | 270/3024 | 118/1437 | 40/478 | chr12 | 89497325 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:89466812 | T | C | 1 | a0001c0004 | 1 | HG03130.hp2 | synonymous_variant | LOW | c.990A>G | p.Pro330Pro | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 9/12 | 1142/3024 | 990/1437 | 330/478 | chr12 | 89466812 | |||
| chr12:89470385 | G | A | 1 | a0001c0002 | 5 | HG00558.hp2 HG00621.hp2 HG02040.hp1 others(2): Show |
synonymous_variant | LOW | c.786C>T | p.Leu262Leu | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 7/12 | 938/3024 | 786/1437 | 262/478 | chr12 | 89470385 | |||
| chr12:89470487 | G | A | 1 | a0001c0005 | 1 | NA18962.hp1 | synonymous_variant | LOW | c.684C>T | p.Ser228Ser | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 7/12 | 836/3024 | 684/1437 | 228/478 | chr12 | 89470487 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:89419756 | CA | C | 2 | a0001c0001t0008 a0001c0001t0012 |
4 | HG02486.hp1 HG02622.hp2 HG02717.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1396delT | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 12/12 | 1396 | chr12 | 89419756 | ||||||
| chr12:89419900 | A | G | 1 | a0001c0001t0005 | 3 | HG02615.hp1 HG03540.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1253T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 12/12 | 1253 | chr12 | 89419900 | ||||||
| chr12:89419970 | A | C | 1 | a0001c0001t0004 | 3 | HG00639.hp1 HG01891.hp1 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1183T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 12/12 | 1183 | chr12 | 89419970 | ||||||
| chr12:89420270 | AAGTACTT others(7): Show |
A | 1 | a0001c0001t0013 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*869_*882delAAATAG others(8): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 12/12 | 869 | chr12 | 89420270 | ||||||
| chr12:89420456 | A | T | 1 | a0001c0001t0010 | 2 | HG02258.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*697T>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 12/12 | 697 | chr12 | 89420456 | ||||||
| chr12:89420457 | T | C | 1 | a0001c0001t0007 | 3 | NA18959.hp1 NA18989.hp1 NA18999.hp1 |
3_prime_UTR_variant | MODIFIER | c.*696A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 12/12 | 696 | chr12 | 89420457 | ||||||
| chr12:89420501 | T | C | 1 | a0001c0001t0003 | 4 | HG02280.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*652A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 12/12 | 652 | chr12 | 89420501 | ||||||
| chr12:89420838 | G | A | 1 | a0001c0001t0006 | 3 | HG01070.hp2 HG01361.hp1 HG01891.hp2 |
3_prime_UTR_variant | MODIFIER | c.*315C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 12/12 | 315 | chr12 | 89420838 | ||||||
| chr12:89420908 | ATCACT | A | 4 | a0001c0001t0002 a0001c0001t0007 a0001c0002t0002 others(1): Show |
56 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*240_*244delAGTGA | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 12/12 | 240 | chr12 | 89420908 | ||||||
| chr12:89421141 | T | C | 1 | a0001c0001t0014 | 1 | NA18951.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 12/12 | 12 | chr12 | 89421141 | ||||||
| chr12:89525903 | G | A | 2 | a0001c0001t0008 a0001c0001t0015 |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-8C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 1/12 | 8 | chr12 | 89525903 | ||||||
| chr12:89525926 | G | A | 1 | a0001c0001t0011 | 2 | HG01123.hp2 HG02451.hp1 |
5_prime_UTR_variant | MODIFIER | c.-31C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 1/12 | 31 | chr12 | 89525926 | ||||||
| chr12:89526025 | A | G | 1 | a0001c0001t0009 | 2 | HG02647.hp2 HG02895.hp1 |
5_prime_UTR_variant | MODIFIER | c.-130T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 1/12 | 130 | chr12 | 89526025 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:89421434 | G | A | 1 | a0001c0001t0001g0302 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1333-177C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 11/11 | chr12 | 89421434 | |||||||
| chr12:89421516 | A | C | 1 | a0001c0001t0001g0109 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1333-259T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 11/11 | chr12 | 89421516 | |||||||
| chr12:89421617 | G | A | 4 | a0001c0001t0003g0042 a0001c0001t0003g0205 a0001c0001t0003g0350 others(1): Show |
4 | HG02280.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1333-360C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 11/11 | chr12 | 89421617 | |||||||
| chr12:89421637 | C | A | 90 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0029 others(87): Show |
91 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.1333-380G>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 11/11 | chr12 | 89421637 | |||||||
| chr12:89421979 | T | C | 33 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0018 others(30): Show |
34 | HG00621.hp1 HG00733.hp1 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.1333-722A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 11/11 | chr12 | 89421979 | |||||||
| chr12:89422040 | CT | C | 91 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0029 others(88): Show |
92 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.1333-784delA | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 11/11 | chr12 | 89422040 | |||||||
| chr12:89422050 | T | A | 24 | a0001c0001t0001g0004 a0001c0001t0001g0035 a0001c0001t0001g0036 others(21): Show |
25 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(22): Show |
intron_variant | MODIFIER | c.1333-793A>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 11/11 | chr12 | 89422050 | |||||||
| chr12:89422077 | T | C | 68 | a0001c0001t0001g0004 a0001c0001t0001g0035 a0001c0001t0001g0036 others(65): Show |
69 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.1333-820A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 11/11 | chr12 | 89422077 | |||||||
| chr12:89422094 | C | T | 3 | a0001c0001t0001g0233 a0001c0001t0010g0234 a0001c0001t0010g0235 |
3 | HG02258.hp2 HG02922.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1333-837G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 11/11 | chr12 | 89422094 | |||||||
| chr12:89422110 | G | A | 3 | a0001c0001t0001g0027 a0001c0001t0001g0107 a0001c0001t0001g0108 |
3 | HG01496.hp1 HG02896.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1333-853C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 11/11 | chr12 | 89422110 | |||||||
| chr12:89422128 | A | G | 6 | a0001c0001t0001g0066 a0001c0001t0001g0068 a0001c0001t0008g0359 others(3): Show |
6 | HG02257.hp1 HG02486.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1333-871T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 11/11 | chr12 | 89422128 | |||||||
| chr12:89422156 | C | A | 1 | a0001c0001t0001g0215 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1333-899G>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 11/11 | chr12 | 89422156 | |||||||
| chr12:89422328 | T | A | 1 | a0001c0001t0001g0060 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1333-1071A>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 11/11 | chr12 | 89422328 | |||||||
| chr12:89422409 | T | A | 1 | a0001c0001t0001g0199 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1333-1152A>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 11/11 | chr12 | 89422409 | |||||||
| chr12:89422478 | A | C | 1 | a0001c0001t0001g0266 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1333-1221T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 11/11 | chr12 | 89422478 | |||||||
| chr12:89422504 | TC | T | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02486.hp1 HG02622.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1333-1248delG | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 11/11 | chr12 | 89422504 | |||||||
| chr12:89422634 | G | A | 2 | a0001c0001t0001g0104 a0001c0001t0001g0105 |
2 | HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1333-1377C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 11/11 | chr12 | 89422634 | |||||||
| chr12:89422649 | T | G | 2 | a0001c0001t0001g0066 a0001c0001t0001g0068 |
2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1333-1392A>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 11/11 | chr12 | 89422649 | |||||||
| chr12:89422666 | T | A | 94 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0029 others(91): Show |
95 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.1333-1409A>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 11/11 | chr12 | 89422666 | |||||||
| chr12:89422915 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1333-1658A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 11/11 | chr12 | 89422915 | |||||||
| chr12:89422985 | C | T | 2 | a0001c0001t0001g0250 a0001c0001t0001g0254 |
2 | HG01257.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1333-1728G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 11/11 | chr12 | 89422985 | |||||||
| chr12:89423063 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1333-1806C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 11/11 | chr12 | 89423063 | |||||||
| chr12:89423133 | T | TGGGAGAT others(10): Show |
4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02486.hp1 HG02622.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1333-1877_1333-187 others(21): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 11/11 | chr12 | 89423133 | |||||||
| chr12:89423134 | A | G | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02486.hp1 HG02622.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1333-1877T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 11/11 | chr12 | 89423134 | |||||||
| chr12:89423165 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1333-1908G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 11/11 | chr12 | 89423165 | |||||||
| chr12:89423240 | C | T | 1 | a0001c0001t0002g0152 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1332+1921G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 11/11 | chr12 | 89423240 | |||||||
| chr12:89423302 | A | T | 273 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(270): Show |
277 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(274): Show |
intron_variant | MODIFIER | c.1332+1859T>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 11/11 | chr12 | 89423302 | |||||||
| chr12:89423365 | T | C | 3 | a0001c0001t0004g0040 a0001c0001t0004g0284 a0001c0001t0004g0287 |
3 | HG00639.hp1 HG01891.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1332+1796A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 11/11 | chr12 | 89423365 | |||||||
| chr12:89423587 | C | T | 90 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0029 others(87): Show |
91 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.1332+1574G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 11/11 | chr12 | 89423587 | |||||||
| chr12:89423694 | C | T | 2 | a0001c0001t0001g0066 a0001c0001t0001g0068 |
2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1332+1467G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 11/11 | chr12 | 89423694 | |||||||
| chr12:89423766 | A | G | 1 | a0001c0001t0001g0077 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1332+1395T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 11/11 | chr12 | 89423766 | |||||||
| chr12:89423920 | T | C | 35 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0012 others(32): Show |
36 | HG00621.hp1 HG00733.hp1 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.1332+1241A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 11/11 | chr12 | 89423920 | |||||||
| chr12:89423992 | C | T | 4 | a0001c0001t0003g0042 a0001c0001t0003g0205 a0001c0001t0003g0350 others(1): Show |
4 | HG02280.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1332+1169G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 11/11 | chr12 | 89423992 | |||||||
| chr12:89424227 | G | GT | 56 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0021 others(53): Show |
56 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1332+933dupA | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 11/11 | chr12 | 89424227 | |||||||
| chr12:89424233 | C | A | 56 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0021 others(53): Show |
56 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1332+928G>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 11/11 | chr12 | 89424233 | |||||||
| chr12:89424245 | T | G | 211 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(208): Show |
214 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.1332+916A>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 11/11 | chr12 | 89424245 | |||||||
| chr12:89424369 | T | C | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02486.hp1 HG02622.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1332+792A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 11/11 | chr12 | 89424369 | |||||||
| chr12:89424493 | C | G | 1 | a0001c0001t0002g0125 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1332+668G>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 11/11 | chr12 | 89424493 | |||||||
| chr12:89424512 | T | C | 290 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(287): Show |
294 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(291): Show |
intron_variant | MODIFIER | c.1332+649A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 11/11 | chr12 | 89424512 | |||||||
| chr12:89424851 | T | C | 1 | a0001c0001t0001g0063 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1332+310A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 11/11 | chr12 | 89424851 | |||||||
| chr12:89424950 | T | C | 126 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(123): Show |
128 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.1332+211A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 11/11 | chr12 | 89424950 | |||||||
| chr12:89424955 | G | C | 2 | a0001c0001t0001g0053 a0001c0001t0001g0064 |
2 | HG00741.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.1332+206C>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 11/11 | chr12 | 89424955 | |||||||
| chr12:89425095 | T | C | 1 | a0001c0001t0001g0098 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1332+66A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 11/11 | chr12 | 89425095 | |||||||
| chr12:89425389 | C | T | 2 | a0001c0001t0001g0250 a0001c0001t0001g0254 |
2 | HG01257.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1114-10G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89425389 | |||||||
| chr12:89425471 | C | A | 1 | a0001c0001t0001g0280 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1114-92G>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89425471 | |||||||
| chr12:89425629 | T | C | 2 | a0001c0001t0004g0284 a0001c0001t0004g0287 |
2 | HG01891.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1114-250A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89425629 | |||||||
| chr12:89425717 | G | A | 2 | a0001c0001t0001g0198 a0001c0001t0001g0201 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1114-338C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89425717 | |||||||
| chr12:89425755 | G | C | 1 | a0001c0001t0001g0353 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1114-376C>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89425755 | |||||||
| chr12:89425925 | G | A | 9 | a0001c0001t0002g0051 a0001c0001t0002g0112 a0001c0001t0002g0114 others(6): Show |
9 | HG02132.hp2 HG02523.hp2 NA18945.hp1 others(6): Show |
intron_variant | MODIFIER | c.1114-546C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89425925 | |||||||
| chr12:89426034 | T | C | 1 | a0001c0001t0002g0307 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1114-655A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89426034 | |||||||
| chr12:89426053 | G | A | 68 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0029 others(65): Show |
69 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.1114-674C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89426053 | |||||||
| chr12:89426298 | C | T | 7 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0182 others(4): Show |
7 | HG02135.hp1 NA18944.hp2 NA18947.hp1 others(4): Show |
intron_variant | MODIFIER | c.1114-919G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89426298 | |||||||
| chr12:89426696 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1114-1317G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89426696 | |||||||
| chr12:89426780 | C | T | 1 | a0001c0001t0001g0241 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1114-1401G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89426780 | |||||||
| chr12:89426926 | C | A | 32 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0018 others(29): Show |
33 | HG00621.hp1 HG00733.hp1 HG01192.hp1 others(30): Show |
intron_variant | MODIFIER | c.1114-1547G>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89426926 | |||||||
| chr12:89427289 | T | C | 78 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0034 others(75): Show |
79 | HG00099.hp2 HG00597.hp2 HG01074.hp2 others(76): Show |
intron_variant | MODIFIER | c.1114-1910A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89427289 | |||||||
| chr12:89427335 | T | C | 3 | a0001c0001t0002g0163 a0001c0001t0002g0164 a0001c0001t0002g0165 |
3 | NA19087.hp1 NA19090.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1114-1956A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89427335 | |||||||
| chr12:89427457 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1114-2078G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89427457 | |||||||
| chr12:89427543 | A | C | 3 | a0001c0001t0004g0040 a0001c0001t0004g0284 a0001c0001t0004g0287 |
3 | HG00639.hp1 HG01891.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1114-2164T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89427543 | |||||||
| chr12:89427589 | T | A | 3 | a0001c0001t0006g0226 a0001c0001t0006g0227 a0001c0001t0006g0228 |
3 | HG01070.hp2 HG01361.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.1114-2210A>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89427589 | |||||||
| chr12:89427814 | C | T | 3 | a0001c0001t0004g0040 a0001c0001t0004g0284 a0001c0001t0004g0287 |
3 | HG00639.hp1 HG01891.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1114-2435G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89427814 | |||||||
| chr12:89427925 | T | C | 4 | a0001c0001t0003g0042 a0001c0001t0003g0205 a0001c0001t0003g0350 others(1): Show |
4 | HG02280.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1114-2546A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89427925 | |||||||
| chr12:89428210 | A | C | 2 | a0001c0001t0001g0252 a0001c0001t0001g0260 |
2 | HG01074.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.1114-2831T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89428210 | |||||||
| chr12:89428376 | C | T | 5 | a0001c0001t0001g0070 a0001c0001t0001g0074 a0001c0001t0001g0075 others(2): Show |
5 | HG00673.hp2 HG00735.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.1114-2997G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89428376 | |||||||
| chr12:89428406 | G | T | 3 | a0001c0001t0001g0121 a0001c0001t0001g0161 a0001c0001t0001g0352 |
3 | HG02723.hp2 HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1114-3027C>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89428406 | |||||||
| chr12:89428537 | A | T | 130 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(127): Show |
132 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.1114-3158T>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89428537 | |||||||
| chr12:89428727 | T | C | 4 | a0001c0001t0003g0042 a0001c0001t0003g0205 a0001c0001t0003g0350 others(1): Show |
4 | HG02280.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1114-3348A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89428727 | |||||||
| chr12:89428747 | G | A | 68 | a0001c0001t0001g0004 a0001c0001t0001g0035 a0001c0001t0001g0036 others(65): Show |
69 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.1114-3368C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89428747 | |||||||
| chr12:89428758 | A | G | 3 | a0001c0001t0001g0027 a0001c0001t0001g0107 a0001c0001t0001g0108 |
3 | HG01496.hp1 HG02896.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1114-3379T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89428758 | |||||||
| chr12:89428769 | G | A | 4 | a0001c0001t0001g0301 a0001c0001t0001g0304 a0001c0001t0001g0305 others(1): Show |
4 | HG00597.hp2 NA18956.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.1114-3390C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89428769 | |||||||
| chr12:89428888 | G | A | 4 | a0001c0001t0003g0042 a0001c0001t0003g0205 a0001c0001t0003g0350 others(1): Show |
4 | HG02280.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1114-3509C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89428888 | |||||||
| chr12:89428915 | G | T | 1 | a0001c0001t0001g0313 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1114-3536C>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89428915 | |||||||
| chr12:89429016 | A | G | 2 | a0001c0001t0001g0066 a0001c0001t0001g0068 |
2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1114-3637T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89429016 | |||||||
| chr12:89429092 | T | C | 1 | a0001c0001t0001g0005 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1114-3713A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89429092 | |||||||
| chr12:89429321 | T | C | 7 | a0001c0001t0001g0006 a0001c0001t0001g0086 a0001c0001t0001g0230 others(4): Show |
8 | HG02027.hp2 HG02129.hp1 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.1114-3942A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89429321 | |||||||
| chr12:89429419 | T | C | 2 | a0001c0001t0001g0066 a0001c0001t0001g0068 |
2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1114-4040A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89429419 | |||||||
| chr12:89429435 | A | G | 1 | a0001c0001t0001g0280 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1114-4056T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89429435 | |||||||
| chr12:89429625 | C | T | 2 | a0001c0001t0001g0066 a0001c0001t0001g0068 |
2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1114-4246G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89429625 | |||||||
| chr12:89429949 | A | G | 2 | a0001c0001t0001g0191 a0001c0001t0002g0134 |
2 | HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1114-4570T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89429949 | |||||||
| chr12:89430084 | G | T | 3 | a0001c0001t0001g0066 a0001c0001t0001g0068 a0001c0001t0004g0284 |
3 | HG01891.hp1 HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1114-4705C>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89430084 | |||||||
| chr12:89430146 | A | AGAAATCC others(324): Show |
2 | a0001c0001t0001g0304 a0001c0001t0001g0305 |
2 | HG00597.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.1114-4768_1114-476 others(335): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89430146 | |||||||
| chr12:89430153 | C | T | 1 | a0001c0001t0002g0282 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1114-4774G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89430153 | |||||||
| chr12:89430248 | C | T | 2 | a0001c0001t0001g0220 a0001c0001t0015g0358 |
2 | HG02809.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1114-4869G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89430248 | |||||||
| chr12:89430263 | C | T | 162 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(159): Show |
164 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.1114-4884G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89430263 | |||||||
| chr12:89430318 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1114-4939A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89430318 | |||||||
| chr12:89430353 | T | G | 1 | a0001c0001t0001g0283 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1114-4974A>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89430353 | |||||||
| chr12:89430532 | G | A | 10 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0055 others(7): Show |
11 | HG01070.hp2 HG01361.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.1114-5153C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89430532 | |||||||
| chr12:89430548 | A | G | 9 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(6): Show |
9 | HG01192.hp1 HG02055.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1114-5169T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89430548 | |||||||
| chr12:89430592 | C | T | 3 | a0001c0001t0006g0226 a0001c0001t0006g0227 a0001c0001t0006g0228 |
3 | HG01070.hp2 HG01361.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.1114-5213G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89430592 | |||||||
| chr12:89430750 | C | T | 1 | a0001c0001t0001g0122 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1114-5371G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89430750 | |||||||
| chr12:89430856 | C | T | 63 | a0001c0001t0001g0103 a0001c0001t0001g0120 a0001c0001t0001g0122 others(60): Show |
63 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.1114-5477G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89430856 | |||||||
| chr12:89431008 | T | C | 3 | a0001c0001t0001g0059 a0001c0001t0001g0062 a0001c0001t0001g0100 |
3 | HG03017.hp1 HG04115.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1114-5629A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89431008 | |||||||
| chr12:89431131 | G | A | 21 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(18): Show |
21 | HG00621.hp1 HG00733.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.1114-5752C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89431131 | |||||||
| chr12:89431185 | A | C | 1 | a0001c0001t0001g0191 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1114-5806T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89431185 | |||||||
| chr12:89431337 | G | T | 23 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0023 others(20): Show |
24 | HG00621.hp1 HG00733.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.1114-5958C>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89431337 | |||||||
| chr12:89431345 | G | T | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
175 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.1114-5966C>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89431345 | |||||||
| chr12:89431427 | A | C | 7 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(4): Show |
7 | HG01192.hp1 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1114-6048T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89431427 | |||||||
| chr12:89431434 | T | TAC | 94 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(91): Show |
95 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.1114-6057_1114-605 others(6): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89431434 | |||||||
| chr12:89431434 | TAC | T | 10 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(7): Show |
10 | HG00673.hp1 HG00673.hp2 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.1114-6057_1114-605 others(6): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89431434 | |||||||
| chr12:89431456 | C | T | 1 | a0001c0001t0001g0338 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1114-6077G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89431456 | |||||||
| chr12:89431614 | G | A | 1 | a0001c0001t0002g0232 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1114-6235C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89431614 | |||||||
| chr12:89431983 | T | C | 2 | a0001c0001t0001g0268 a0001c0001t0001g0271 |
2 | HG00408.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1114-6604A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89431983 | |||||||
| chr12:89432035 | C | G | 1 | a0001c0001t0003g0351 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1114-6656G>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89432035 | |||||||
| chr12:89432148 | T | C | 88 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0018 others(85): Show |
89 | HG00099.hp2 HG00597.hp2 HG00639.hp1 others(86): Show |
intron_variant | MODIFIER | c.1114-6769A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89432148 | |||||||
| chr12:89432255 | A | G | 1 | a0001c0001t0001g0230 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1114-6876T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89432255 | |||||||
| chr12:89432264 | T | C | 1 | a0001c0001t0001g0236 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1114-6885A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89432264 | |||||||
| chr12:89432334 | C | T | 2 | a0001c0001t0001g0034 a0003c0006t0001g0322 |
2 | HG02165.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.1114-6955G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89432334 | |||||||
| chr12:89432335 | C | G | 95 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0018 others(92): Show |
96 | HG00099.hp2 HG00597.hp2 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.1114-6956G>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89432335 | |||||||
| chr12:89432381 | C | G | 1 | a0001c0001t0001g0144 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1114-7002G>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89432381 | |||||||
| chr12:89432383 | TA | T | 77 | a0001c0001t0001g0006 a0001c0001t0001g0027 a0001c0001t0001g0029 others(74): Show |
78 | HG00323.hp1 HG00408.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.1114-7005delT | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89432383 | |||||||
| chr12:89432383 | TAA | T | 31 | a0001c0001t0001g0016 a0001c0001t0001g0035 a0001c0001t0001g0036 others(28): Show |
31 | HG00738.hp1 HG01099.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.1114-7006_1114-700 others(6): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89432383 | |||||||
| chr12:89432383 | TAAA | T | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(154): Show |
162 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.1114-7007_1114-700 others(7): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89432383 | |||||||
| chr12:89432383 | TAAAA | T | 74 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0034 others(71): Show |
75 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.1114-7008_1114-700 others(8): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89432383 | |||||||
| chr12:89432384 | A | T | 1 | a0001c0001t0001g0144 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1114-7005T>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89432384 | |||||||
| chr12:89432385 | A | C | 1 | a0001c0001t0001g0144 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1114-7006T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89432385 | |||||||
| chr12:89432386 | A | T | 1 | a0001c0001t0001g0144 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1114-7007T>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89432386 | |||||||
| chr12:89432387 | A | T | 1 | a0001c0001t0001g0144 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1114-7008T>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89432387 | |||||||
| chr12:89432433 | G | T | 270 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(267): Show |
276 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(273): Show |
intron_variant | MODIFIER | c.1114-7054C>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89432433 | |||||||
| chr12:89432516 | T | C | 45 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(42): Show |
48 | HG00323.hp2 HG00423.hp2 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.1114-7137A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89432516 | |||||||
| chr12:89432677 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1114-7298T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89432677 | |||||||
| chr12:89432725 | G | A | 23 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0023 others(20): Show |
24 | HG00621.hp1 HG00733.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.1114-7346C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89432725 | |||||||
| chr12:89432761 | G | C | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1114-7382C>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89432761 | |||||||
| chr12:89433067 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1114-7688C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89433067 | |||||||
| chr12:89433129 | C | G | 3 | a0001c0001t0005g0043 a0001c0001t0005g0044 a0001c0001t0005g0045 |
3 | HG02615.hp1 HG03540.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1114-7750G>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89433129 | |||||||
| chr12:89433166 | A | AT | 6 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0084 others(3): Show |
6 | HG00639.hp1 HG02055.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1114-7788dupA | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89433166 | |||||||
| chr12:89433333 | G | A | 6 | a0001c0001t0001g0004 a0001c0001t0001g0104 a0001c0001t0001g0105 others(3): Show |
7 | HG02486.hp1 HG02723.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1114-7954C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89433333 | |||||||
| chr12:89433511 | T | C | 1 | a0001c0001t0001g0354 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1114-8132A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89433511 | |||||||
| chr12:89433913 | C | T | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1114-8534G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89433913 | |||||||
| chr12:89434094 | T | A | 1 | a0001c0001t0001g0121 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1114-8715A>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89434094 | |||||||
| chr12:89434120 | G | A | 4 | a0001c0001t0001g0291 a0001c0001t0001g0308 a0001c0001t0001g0309 others(1): Show |
4 | HG01074.hp2 HG01106.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.1114-8741C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89434120 | |||||||
| chr12:89434266 | T | C | 6 | a0001c0001t0001g0300 a0001c0001t0001g0302 a0001c0001t0001g0320 others(3): Show |
6 | HG02280.hp1 HG02615.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1114-8887A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89434266 | |||||||
| chr12:89434296 | A | C | 2 | a0001c0001t0001g0345 a0001c0001t0002g0307 |
2 | HG02074.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1114-8917T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89434296 | |||||||
| chr12:89434364 | C | A | 45 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(42): Show |
48 | HG00323.hp2 HG00423.hp2 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.1114-8985G>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89434364 | |||||||
| chr12:89434402 | C | A | 1 | a0001c0001t0002g0152 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1114-9023G>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89434402 | |||||||
| chr12:89434472 | T | C | 1 | a0001c0001t0001g0343 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1114-9093A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89434472 | |||||||
| chr12:89434595 | C | T | 3 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0003g0205 |
3 | HG02280.hp2 HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1114-9216G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89434595 | |||||||
| chr12:89434794 | C | T | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(273): Show |
282 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(279): Show |
intron_variant | MODIFIER | c.1114-9415G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89434794 | |||||||
| chr12:89434796 | C | T | 1 | a0001c0001t0001g0336 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1114-9417G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89434796 | |||||||
| chr12:89434814 | A | G | 93 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0018 others(90): Show |
94 | HG00099.hp2 HG00597.hp2 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.1114-9435T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89434814 | |||||||
| chr12:89434948 | T | A | 1 | a0001c0001t0002g0134 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1114-9569A>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89434948 | |||||||
| chr12:89434954 | C | T | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
283 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.1114-9575G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89434954 | |||||||
| chr12:89434978 | T | A | 5 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0084 others(2): Show |
5 | HG02055.hp1 HG02145.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1114-9599A>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89434978 | |||||||
| chr12:89435059 | C | T | 1 | a0001c0001t0001g0223 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1114-9680G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89435059 | |||||||
| chr12:89435179 | C | CT | 14 | a0001c0001t0001g0006 a0001c0001t0001g0086 a0001c0001t0001g0230 others(11): Show |
15 | HG02027.hp2 HG02080.hp2 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.1114-9801dupA | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89435179 | |||||||
| chr12:89435179 | CT | C | 265 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(262): Show |
271 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(268): Show |
intron_variant | MODIFIER | c.1114-9801delA | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89435179 | |||||||
| chr12:89435385 | T | C | 1 | a0001c0001t0001g0357 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1114-10006A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89435385 | |||||||
| chr12:89435402 | A | G | 2 | a0001c0001t0009g0008 a0001c0001t0009g0009 |
2 | HG02647.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1114-10023T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89435402 | |||||||
| chr12:89435670 | A | C | 9 | a0001c0001t0001g0004 a0001c0001t0001g0104 a0001c0001t0001g0105 others(6): Show |
10 | HG02280.hp2 HG02486.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1114-10291T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89435670 | |||||||
| chr12:89435687 | T | C | 1 | a0001c0001t0001g0063 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1114-10308A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89435687 | |||||||
| chr12:89435693 | C | T | 92 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0018 others(89): Show |
93 | HG00099.hp2 HG00597.hp2 HG00639.hp1 others(90): Show |
intron_variant | MODIFIER | c.1114-10314G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89435693 | |||||||
| chr12:89435767 | T | C | 1 | a0001c0001t0001g0026 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1114-10388A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89435767 | |||||||
| chr12:89435846 | G | A | 1 | a0001c0001t0001g0160 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1114-10467C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89435846 | |||||||
| chr12:89435882 | C | T | 1 | a0001c0001t0001g0010 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1114-10503G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89435882 | |||||||
| chr12:89435929 | G | T | 4 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(1): Show |
4 | HG01109.hp1 HG02630.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1114-10550C>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89435929 | |||||||
| chr12:89435951 | G | T | 14 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0192 others(11): Show |
14 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.1114-10572C>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89435951 | |||||||
| chr12:89435984 | C | T | 1 | a0001c0001t0001g0010 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1114-10605G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89435984 | |||||||
| chr12:89435985 | G | A | 5 | a0001c0002t0001g0244 a0001c0002t0001g0262 a0001c0002t0001g0263 others(2): Show |
5 | HG00558.hp2 HG00621.hp2 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.1114-10606C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89435985 | |||||||
| chr12:89435995 | A | C | 1 | a0001c0001t0001g0200 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1114-10616T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89435995 | |||||||
| chr12:89436185 | T | C | 2 | a0001c0001t0001g0104 a0001c0001t0001g0105 |
2 | HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1114-10806A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89436185 | |||||||
| chr12:89436358 | G | T | 6 | a0001c0001t0001g0300 a0001c0001t0001g0302 a0001c0001t0001g0320 others(3): Show |
6 | HG02280.hp1 HG02615.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1114-10979C>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89436358 | |||||||
| chr12:89436410 | C | G | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | HG01346.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.1114-11031G>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89436410 | |||||||
| chr12:89436645 | C | T | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1114-11266G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89436645 | |||||||
| chr12:89436663 | G | C | 45 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(42): Show |
48 | HG00323.hp2 HG00423.hp2 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.1114-11284C>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89436663 | |||||||
| chr12:89436671 | T | C | 3 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 |
3 | HG01192.hp1 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1114-11292A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89436671 | |||||||
| chr12:89436680 | T | C | 2 | a0001c0001t0001g0121 a0001c0001t0001g0161 |
2 | HG02723.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1114-11301A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89436680 | |||||||
| chr12:89436713 | C | CA | 8 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(5): Show |
8 | HG01109.hp1 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1114-11335dupT | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89436713 | |||||||
| chr12:89436735 | A | C | 4 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(1): Show |
4 | HG01109.hp1 HG02630.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1114-11356T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89436735 | |||||||
| chr12:89436746 | A | G | 82 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0018 others(79): Show |
83 | HG00099.hp2 HG00597.hp2 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.1114-11367T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89436746 | |||||||
| chr12:89436834 | A | C | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
283 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.1114-11455T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89436834 | |||||||
| chr12:89436937 | C | T | 1 | a0001c0005t0002g0138 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1114-11558G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89436937 | |||||||
| chr12:89436943 | T | C | 84 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0018 others(81): Show |
85 | HG00099.hp2 HG00597.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.1114-11564A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89436943 | |||||||
| chr12:89437071 | A | G | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1114-11692T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89437071 | |||||||
| chr12:89437093 | C | T | 76 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0034 others(73): Show |
78 | HG00099.hp2 HG00597.hp2 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.1114-11714G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89437093 | |||||||
| chr12:89437101 | C | T | 1 | a0001c0004t0001g0264 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1114-11722G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89437101 | |||||||
| chr12:89437137 | C | T | 2 | a0001c0001t0001g0252 a0001c0001t0001g0260 |
2 | HG01074.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.1114-11758G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89437137 | |||||||
| chr12:89437194 | C | T | 1 | a0001c0001t0001g0151 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1114-11815G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89437194 | |||||||
| chr12:89437305 | G | A | 6 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0084 others(3): Show |
6 | HG00639.hp1 HG02055.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1114-11926C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89437305 | |||||||
| chr12:89437414 | A | C | 5 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0084 others(2): Show |
5 | HG00639.hp1 HG02055.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.1114-12035T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89437414 | |||||||
| chr12:89437590 | T | C | 1 | a0001c0001t0001g0275 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1114-12211A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89437590 | |||||||
| chr12:89437636 | T | A | 1 | a0001c0001t0002g0164 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1114-12257A>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89437636 | |||||||
| chr12:89437652 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1114-12273T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89437652 | |||||||
| chr12:89437813 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1114-12434G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89437813 | |||||||
| chr12:89437817 | A | G | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
283 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.1114-12438T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89437817 | |||||||
| chr12:89437861 | A | C | 3 | a0001c0001t0006g0226 a0001c0001t0006g0227 a0001c0001t0006g0228 |
3 | HG01070.hp2 HG01361.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.1114-12482T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89437861 | |||||||
| chr12:89437886 | A | G | 1 | a0001c0001t0001g0004 | 2 | HG02723.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1114-12507T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89437886 | |||||||
| chr12:89438050 | C | CA | 12 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0047 others(9): Show |
13 | HG01192.hp1 HG02135.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.1114-12672dupT | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89438050 | |||||||
| chr12:89438050 | CA | C | 36 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0026 others(33): Show |
37 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.1114-12672delT | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89438050 | |||||||
| chr12:89438068 | T | A | 6 | a0001c0001t0001g0054 a0001c0001t0001g0061 a0001c0001t0001g0069 others(3): Show |
6 | NA18942.hp1 NA18962.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1114-12689A>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89438068 | |||||||
| chr12:89438288 | T | G | 6 | a0001c0001t0001g0107 a0001c0001t0008g0359 a0001c0001t0008g0360 others(3): Show |
6 | HG02486.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1114-12909A>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89438288 | |||||||
| chr12:89438322 | T | C | 6 | a0001c0001t0001g0031 a0001c0001t0001g0237 a0001c0001t0001g0251 others(3): Show |
6 | HG01074.hp1 HG01099.hp1 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.1114-12943A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89438322 | |||||||
| chr12:89438382 | G | A | 1 | a0001c0001t0001g0352 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1114-13003C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89438382 | |||||||
| chr12:89438458 | A | AAAAC | 3 | a0001c0001t0002g0019 a0001c0001t0002g0152 a0001c0001t0002g0162 |
3 | HG03831.hp2 NA18954.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1114-13083_1114-13 others(10): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89438458 | |||||||
| chr12:89438458 | AAAAC | A | 3 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 |
3 | HG01192.hp1 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1114-13083_1114-13 others(10): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89438458 | |||||||
| chr12:89438646 | C | T | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(190): Show |
198 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(195): Show |
intron_variant | MODIFIER | c.1114-13267G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89438646 | |||||||
| chr12:89439165 | A | C | 1 | a0001c0001t0001g0111 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1114-13786T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89439165 | |||||||
| chr12:89439451 | C | T | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1114-14072G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89439451 | |||||||
| chr12:89439501 | G | A | 1 | a0001c0001t0001g0281 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1114-14122C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89439501 | |||||||
| chr12:89439561 | T | C | 75 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0289 others(72): Show |
76 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.1114-14182A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89439561 | |||||||
| chr12:89439597 | T | G | 3 | a0001c0001t0001g0004 a0001c0001t0001g0107 a0001c0001t0012g0106 |
4 | HG02486.hp1 HG02723.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1114-14218A>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89439597 | |||||||
| chr12:89439966 | C | T | 1 | a0001c0001t0001g0170 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1114-14587G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89439966 | |||||||
| chr12:89440134 | A | C | 5 | a0001c0001t0001g0233 a0001c0001t0001g0242 a0001c0001t0001g0246 others(2): Show |
5 | HG02258.hp2 HG02451.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1114-14755T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89440134 | |||||||
| chr12:89440336 | C | T | 75 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0289 others(72): Show |
76 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.1114-14957G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89440336 | |||||||
| chr12:89440368 | A | G | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1114-14989T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89440368 | |||||||
| chr12:89440651 | T | A | 75 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0289 others(72): Show |
76 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.1114-15272A>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89440651 | |||||||
| chr12:89440824 | G | C | 14 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0061 others(11): Show |
14 | HG00673.hp2 HG00735.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.1114-15445C>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89440824 | |||||||
| chr12:89440956 | C | T | 3 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0003g0205 |
3 | HG02280.hp2 HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1114-15577G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89440956 | |||||||
| chr12:89441037 | C | T | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(62): Show |
68 | HG00423.hp2 HG00673.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.1114-15658G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89441037 | |||||||
| chr12:89441038 | G | A | 3 | a0001c0001t0006g0226 a0001c0001t0006g0227 a0001c0001t0006g0228 |
3 | HG01070.hp2 HG01361.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.1114-15659C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89441038 | |||||||
| chr12:89441114 | A | G | 4 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0055 others(1): Show |
5 | HG02258.hp1 HG02970.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1114-15735T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89441114 | |||||||
| chr12:89441214 | C | T | 14 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0061 others(11): Show |
14 | HG00673.hp2 HG00735.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.1114-15835G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89441214 | |||||||
| chr12:89441431 | T | C | 3 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0004g0284 |
3 | HG01167.hp2 HG01891.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1114-16052A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89441431 | |||||||
| chr12:89441573 | C | G | 1 | a0001c0001t0001g0098 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1114-16194G>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89441573 | |||||||
| chr12:89441726 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1114-16347G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89441726 | |||||||
| chr12:89441843 | C | T | 3 | a0001c0001t0006g0226 a0001c0001t0006g0227 a0001c0001t0006g0228 |
3 | HG01070.hp2 HG01361.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.1114-16464G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89441843 | |||||||
| chr12:89441883 | T | C | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1114-16504A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89441883 | |||||||
| chr12:89441951 | C | A | 63 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0289 others(60): Show |
64 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.1114-16572G>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89441951 | |||||||
| chr12:89441959 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1114-16580G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89441959 | |||||||
| chr12:89441963 | C | T | 1 | a0001c0001t0004g0284 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1114-16584G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89441963 | |||||||
| chr12:89442055 | A | T | 1 | a0001c0001t0001g0338 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1114-16676T>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89442055 | |||||||
| chr12:89442082 | C | G | 75 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0289 others(72): Show |
76 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.1114-16703G>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89442082 | |||||||
| chr12:89442095 | C | T | 1 | a0001c0001t0001g0011 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1114-16716G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89442095 | |||||||
| chr12:89442123 | G | A | 1 | a0001c0001t0001g0007 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1114-16744C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89442123 | |||||||
| chr12:89442149 | G | A | 75 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0289 others(72): Show |
76 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.1114-16770C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89442149 | |||||||
| chr12:89442348 | G | C | 1 | a0001c0001t0002g0133 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1114-16969C>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89442348 | |||||||
| chr12:89442393 | G | T | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(273): Show |
282 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(279): Show |
intron_variant | MODIFIER | c.1114-17014C>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89442393 | |||||||
| chr12:89442585 | A | C | 1 | a0001c0001t0002g0134 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1113+17053T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89442585 | |||||||
| chr12:89442764 | C | T | 1 | a0001c0001t0001g0011 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1113+16874G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89442764 | |||||||
| chr12:89442895 | G | C | 75 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0289 others(72): Show |
76 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.1113+16743C>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89442895 | |||||||
| chr12:89442900 | G | A | 2 | a0001c0001t0001g0010 a0001c0001t0004g0040 |
2 | HG00639.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1113+16738C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89442900 | |||||||
| chr12:89442937 | A | G | 90 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0023 others(87): Show |
91 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.1113+16701T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89442937 | |||||||
| chr12:89442951 | C | A | 4 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(1): Show |
4 | HG01109.hp1 HG02630.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1113+16687G>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89442951 | |||||||
| chr12:89443282 | C | G | 16 | a0001c0001t0001g0116 a0001c0001t0002g0019 a0001c0001t0002g0020 others(13): Show |
16 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(13): Show |
intron_variant | MODIFIER | c.1113+16356G>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89443282 | |||||||
| chr12:89443404 | T | C | 75 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0289 others(72): Show |
76 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.1113+16234A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89443404 | |||||||
| chr12:89443592 | A | G | 1 | a0001c0001t0001g0240 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1113+16046T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89443592 | |||||||
| chr12:89443699 | G | A | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
283 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.1113+15939C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89443699 | |||||||
| chr12:89443767 | A | T | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1113+15871T>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89443767 | |||||||
| chr12:89443819 | GT | G | 4 | a0001c0001t0001g0352 a0001c0001t0003g0350 a0001c0001t0003g0351 others(1): Show |
4 | HG02647.hp1 HG02922.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1113+15818delA | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89443819 | |||||||
| chr12:89443959 | GAAA | G | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1113+15676_1113+15 others(9): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89443959 | |||||||
| chr12:89444089 | C | A | 3 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0003g0205 |
3 | HG02280.hp2 HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1113+15549G>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89444089 | |||||||
| chr12:89444144 | G | A | 1 | a0001c0001t0001g0330 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1113+15494C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89444144 | |||||||
| chr12:89444232 | A | G | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(270): Show |
279 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(276): Show |
intron_variant | MODIFIER | c.1113+15406T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89444232 | |||||||
| chr12:89444242 | C | T | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1113+15396G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89444242 | |||||||
| chr12:89444283 | C | T | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1113+15355G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89444283 | |||||||
| chr12:89444288 | C | A | 6 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0003g0042 others(3): Show |
6 | HG02572.hp1 HG02615.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1113+15350G>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89444288 | |||||||
| chr12:89444300 | G | A | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(277): Show |
286 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(283): Show |
intron_variant | MODIFIER | c.1113+15338C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89444300 | |||||||
| chr12:89444310 | T | A | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
283 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.1113+15328A>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89444310 | |||||||
| chr12:89444425 | T | A | 1 | a0001c0001t0001g0199 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1113+15213A>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89444425 | |||||||
| chr12:89444587 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1113+15051C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89444587 | |||||||
| chr12:89444613 | A | G | 4 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(1): Show |
4 | HG01109.hp1 HG02630.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1113+15025T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89444613 | |||||||
| chr12:89444647 | T | C | 6 | a0001c0001t0001g0054 a0001c0001t0001g0061 a0001c0001t0001g0069 others(3): Show |
6 | NA18942.hp1 NA18962.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1113+14991A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89444647 | |||||||
| chr12:89444654 | G | C | 1 | a0001c0001t0002g0113 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1113+14984C>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89444654 | |||||||
| chr12:89444707 | G | T | 1 | a0001c0001t0001g0160 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1113+14931C>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89444707 | |||||||
| chr12:89444893 | G | A | 23 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0023 others(20): Show |
24 | HG00621.hp1 HG00733.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.1113+14745C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89444893 | |||||||
| chr12:89444930 | G | A | 1 | a0001c0001t0004g0040 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1113+14708C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89444930 | |||||||
| chr12:89444931 | C | A | 1 | a0001c0001t0004g0040 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1113+14707G>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89444931 | |||||||
| chr12:89445026 | A | T | 75 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0289 others(72): Show |
76 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.1113+14612T>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89445026 | |||||||
| chr12:89445052 | G | A | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(270): Show |
279 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(276): Show |
intron_variant | MODIFIER | c.1113+14586C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89445052 | |||||||
| chr12:89445074 | G | A | 1 | a0001c0001t0001g0050 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1113+14564C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89445074 | |||||||
| chr12:89445110 | C | T | 5 | a0001c0001t0001g0353 a0001c0001t0001g0354 a0001c0001t0001g0355 others(2): Show |
5 | HG00099.hp2 HG01978.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.1113+14528G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89445110 | |||||||
| chr12:89445295 | C | T | 63 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0289 others(60): Show |
64 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.1113+14343G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89445295 | |||||||
| chr12:89445300 | A | T | 1 | a0001c0001t0001g0316 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1113+14338T>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89445300 | |||||||
| chr12:89445465 | C | T | 74 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0289 others(71): Show |
75 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.1113+14173G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89445465 | |||||||
| chr12:89445552 | A | G | 1 | a0001c0001t0001g0029 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1113+14086T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89445552 | |||||||
| chr12:89445686 | C | T | 1 | a0001c0001t0005g0044 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1113+13952G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89445686 | |||||||
| chr12:89445709 | T | C | 8 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0036 others(5): Show |
8 | HG01109.hp1 HG01167.hp2 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.1113+13929A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89445709 | |||||||
| chr12:89445854 | C | T | 1 | a0001c0001t0002g0153 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1113+13784G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89445854 | |||||||
| chr12:89445926 | A | G | 64 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0289 others(61): Show |
65 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.1113+13712T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89445926 | |||||||
| chr12:89445949 | A | G | 75 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0289 others(72): Show |
76 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.1113+13689T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89445949 | |||||||
| chr12:89445987 | A | C | 1 | a0001c0001t0002g0058 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1113+13651T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89445987 | |||||||
| chr12:89446081 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1113+13557C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89446081 | |||||||
| chr12:89446081 | G | T | 1 | a0001c0001t0002g0124 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1113+13557C>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89446081 | |||||||
| chr12:89446196 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1113+13442G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89446196 | |||||||
| chr12:89446456 | C | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0104 a0001c0001t0001g0105 others(2): Show |
6 | HG02486.hp1 HG02723.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1113+13182G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89446456 | |||||||
| chr12:89446457 | G | A | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
195 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.1113+13181C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89446457 | |||||||
| chr12:89446518 | C | T | 3 | a0001c0001t0006g0226 a0001c0001t0006g0227 a0001c0001t0006g0228 |
3 | HG01070.hp2 HG01361.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.1113+13120G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89446518 | |||||||
| chr12:89446576 | G | C | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(62): Show |
68 | HG00423.hp2 HG00673.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.1113+13062C>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89446576 | |||||||
| chr12:89446601 | G | A | 4 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0055 others(1): Show |
5 | HG02258.hp1 HG02970.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1113+13037C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89446601 | |||||||
| chr12:89446806 | T | C | 1 | a0001c0001t0001g0011 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1113+12832A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89446806 | |||||||
| chr12:89446959 | T | C | 1 | a0001c0001t0008g0360 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1113+12679A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89446959 | |||||||
| chr12:89447088 | C | T | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(277): Show |
286 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(283): Show |
intron_variant | MODIFIER | c.1113+12550G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89447088 | |||||||
| chr12:89447173 | T | G | 1 | a0001c0001t0001g0343 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1113+12465A>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89447173 | |||||||
| chr12:89447874 | T | C | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1113+11764A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89447874 | |||||||
| chr12:89447940 | G | A | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(195): Show |
203 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.1113+11698C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89447940 | |||||||
| chr12:89447968 | G | A | 23 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0023 others(20): Show |
24 | HG00621.hp1 HG00733.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.1113+11670C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89447968 | |||||||
| chr12:89448041 | C | A | 2 | a0001c0001t0002g0171 a0001c0001t0002g0208 |
2 | HG02735.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1113+11597G>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89448041 | |||||||
| chr12:89448057 | C | T | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(277): Show |
286 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(283): Show |
intron_variant | MODIFIER | c.1113+11581G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89448057 | |||||||
| chr12:89448170 | T | C | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(195): Show |
203 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.1113+11468A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89448170 | |||||||
| chr12:89448276 | T | C | 75 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0289 others(72): Show |
76 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.1113+11362A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89448276 | |||||||
| chr12:89448317 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1113+11321G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89448317 | |||||||
| chr12:89448345 | A | G | 2 | a0001c0001t0001g0010 a0001c0001t0004g0040 |
2 | HG00639.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1113+11293T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89448345 | |||||||
| chr12:89448590 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1113+11048G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89448590 | |||||||
| chr12:89448679 | T | G | 6 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0003g0042 others(3): Show |
6 | HG02572.hp1 HG02615.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1113+10959A>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89448679 | |||||||
| chr12:89448691 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1113+10947C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89448691 | |||||||
| chr12:89448787 | A | C | 1 | a0001c0001t0001g0301 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1113+10851T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89448787 | |||||||
| chr12:89448821 | A | T | 1 | a0001c0001t0001g0100 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1113+10817T>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89448821 | |||||||
| chr12:89449267 | T | A | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(195): Show |
203 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.1113+10371A>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89449267 | |||||||
| chr12:89449528 | C | A | 1 | a0001c0001t0001g0029 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1113+10110G>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89449528 | |||||||
| chr12:89449549 | A | G | 1 | a0001c0001t0001g0275 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1113+10089T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89449549 | |||||||
| chr12:89449676 | T | C | 1 | a0001c0001t0001g0174 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1113+9962A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89449676 | |||||||
| chr12:89449684 | T | C | 2 | a0001c0001t0001g0060 a0001c0001t0001g0087 |
2 | HG00738.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.1113+9954A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89449684 | |||||||
| chr12:89449782 | TGATAATG others(15): Show |
T | 1 | a0001c0001t0002g0164 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1113+9834_1113+985 others(26): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89449782 | |||||||
| chr12:89449910 | T | C | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
195 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.1113+9728A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89449910 | |||||||
| chr12:89450271 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1113+9367C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89450271 | |||||||
| chr12:89450292 | A | G | 1 | a0001c0001t0004g0284 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1113+9346T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89450292 | |||||||
| chr12:89450497 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1113+9141G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89450497 | |||||||
| chr12:89450539 | G | T | 3 | a0001c0001t0006g0226 a0001c0001t0006g0227 a0001c0001t0006g0228 |
3 | HG01070.hp2 HG01361.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.1113+9099C>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89450539 | |||||||
| chr12:89451072 | C | G | 1 | a0001c0001t0001g0109 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1113+8566G>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89451072 | |||||||
| chr12:89451080 | T | TG | 75 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0289 others(72): Show |
76 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.1113+8557dupC | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89451080 | |||||||
| chr12:89451193 | C | T | 1 | a0001c0001t0002g0140 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1113+8445G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89451193 | |||||||
| chr12:89451234 | A | T | 1 | a0001c0001t0001g0257 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1113+8404T>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89451234 | |||||||
| chr12:89451508 | AATTTT | A | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
195 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.1113+8125_1113+812 others(9): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89451508 | |||||||
| chr12:89451540 | G | A | 2 | a0001c0001t0001g0010 a0001c0001t0004g0040 |
2 | HG00639.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1113+8098C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89451540 | |||||||
| chr12:89451602 | G | A | 2 | a0001c0001t0001g0111 a0001c0001t0001g0303 |
2 | HG01175.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.1113+8036C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89451602 | |||||||
| chr12:89451676 | T | C | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1113+7962A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89451676 | |||||||
| chr12:89452045 | T | G | 6 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0003g0042 others(3): Show |
6 | HG02572.hp1 HG02615.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1113+7593A>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89452045 | |||||||
| chr12:89452167 | G | C | 2 | a0001c0001t0001g0313 a0001c0001t0001g0332 |
2 | HG02071.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1113+7471C>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89452167 | |||||||
| chr12:89452306 | C | T | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1113+7332G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89452306 | |||||||
| chr12:89452395 | T | C | 1 | a0001c0001t0001g0224 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1113+7243A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89452395 | |||||||
| chr12:89452453 | C | T | 75 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0289 others(72): Show |
76 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.1113+7185G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89452453 | |||||||
| chr12:89452524 | TA | T | 6 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0003g0042 others(3): Show |
6 | HG02572.hp1 HG02615.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1113+7113delT | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89452524 | |||||||
| chr12:89452699 | G | A | 75 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0289 others(72): Show |
76 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.1113+6939C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89452699 | |||||||
| chr12:89452716 | C | T | 6 | a0001c0001t0001g0300 a0001c0001t0001g0302 a0001c0001t0001g0320 others(3): Show |
6 | HG02280.hp1 HG02615.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1113+6922G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89452716 | |||||||
| chr12:89452807 | C | T | 3 | a0001c0001t0006g0226 a0001c0001t0006g0227 a0001c0001t0006g0228 |
3 | HG01070.hp2 HG01361.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.1113+6831G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89452807 | |||||||
| chr12:89453048 | T | A | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
283 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.1113+6590A>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89453048 | |||||||
| chr12:89453135 | G | A | 1 | a0001c0001t0001g0011 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1113+6503C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89453135 | |||||||
| chr12:89453179 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1113+6459C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89453179 | |||||||
| chr12:89453330 | A | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0104 a0001c0001t0001g0105 others(2): Show |
6 | HG02486.hp1 HG02723.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1113+6308T>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89453330 | |||||||
| chr12:89453464 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1113+6174G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89453464 | |||||||
| chr12:89453822 | A | G | 3 | a0001c0001t0006g0226 a0001c0001t0006g0227 a0001c0001t0006g0228 |
3 | HG01070.hp2 HG01361.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.1113+5816T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89453822 | |||||||
| chr12:89453848 | A | G | 5 | a0001c0001t0001g0004 a0001c0001t0001g0104 a0001c0001t0001g0105 others(2): Show |
6 | HG02486.hp1 HG02723.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1113+5790T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89453848 | |||||||
| chr12:89453929 | A | C | 2 | a0001c0001t0001g0198 a0001c0001t0001g0201 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1113+5709T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89453929 | |||||||
| chr12:89453992 | C | T | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1113+5646G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89453992 | |||||||
| chr12:89454378 | C | T | 1 | a0001c0001t0001g0011 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1113+5260G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89454378 | |||||||
| chr12:89454410 | G | A | 90 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0023 others(87): Show |
91 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.1113+5228C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89454410 | |||||||
| chr12:89454653 | C | T | 3 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 |
3 | HG01192.hp1 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1113+4985G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89454653 | |||||||
| chr12:89454785 | CCTCT | C | 3 | a0001c0001t0006g0226 a0001c0001t0006g0227 a0001c0001t0006g0228 |
3 | HG01070.hp2 HG01361.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.1113+4849_1113+485 others(8): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89454785 | |||||||
| chr12:89454873 | TAATA | T | 3 | a0001c0001t0001g0200 a0001c0001t0001g0202 a0001c0001t0001g0203 |
3 | HG00642.hp2 HG02004.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.1113+4761_1113+476 others(8): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89454873 | |||||||
| chr12:89454961 | T | TAAAGATT others(313): Show |
4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1113+4676_1113+467 others(324): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89454961 | |||||||
| chr12:89454984 | G | T | 4 | a0001c0001t0001g0022 a0001c0001t0001g0173 a0001c0001t0001g0174 others(1): Show |
4 | HG00621.hp1 NA18952.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.1113+4654C>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89454984 | |||||||
| chr12:89455061 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1113+4577G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89455061 | |||||||
| chr12:89455093 | A | G | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(277): Show |
286 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(283): Show |
intron_variant | MODIFIER | c.1113+4545T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89455093 | |||||||
| chr12:89455297 | T | C | 2 | a0001c0001t0002g0112 a0001c0001t0002g0113 |
2 | HG02132.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.1113+4341A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89455297 | |||||||
| chr12:89455357 | A | G | 3 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0004g0284 |
3 | HG01167.hp2 HG01891.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1113+4281T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89455357 | |||||||
| chr12:89455553 | G | C | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1113+4085C>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89455553 | |||||||
| chr12:89455692 | T | C | 67 | a0001c0001t0001g0077 a0001c0001t0001g0103 a0001c0001t0001g0111 others(64): Show |
67 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.1113+3946A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89455692 | |||||||
| chr12:89455900 | A | G | 8 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0036 others(5): Show |
8 | HG01109.hp1 HG01167.hp2 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.1113+3738T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89455900 | |||||||
| chr12:89455910 | T | C | 2 | a0001c0001t0001g0268 a0001c0001t0001g0271 |
2 | HG00408.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1113+3728A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89455910 | |||||||
| chr12:89455933 | C | G | 3 | a0001c0001t0002g0019 a0001c0001t0002g0152 a0001c0001t0002g0162 |
3 | HG03831.hp2 NA18954.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1113+3705G>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89455933 | |||||||
| chr12:89456002 | C | CTTT | 5 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(2): Show |
5 | HG00639.hp1 HG01109.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1113+3633_1113+363 others(7): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89456002 | |||||||
| chr12:89456006 | T | TTTG | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(196): Show |
203 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.1113+3629_1113+363 others(7): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89456006 | |||||||
| chr12:89456006 | T | TTTGTTG | 27 | a0001c0001t0001g0052 a0001c0001t0001g0070 a0001c0001t0001g0082 others(24): Show |
27 | HG00733.hp1 HG00735.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.1113+3626_1113+363 others(10): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89456006 | |||||||
| chr12:89456006 | TTTG | T | 4 | a0001c0001t0001g0110 a0001c0001t0001g0265 a0001c0001t0001g0273 others(1): Show |
4 | HG00642.hp1 HG01169.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.1113+3629_1113+363 others(7): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89456006 | |||||||
| chr12:89456009 | G | T | 1 | a0001c0001t0004g0040 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1113+3629C>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89456009 | |||||||
| chr12:89456163 | A | G | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(277): Show |
286 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(283): Show |
intron_variant | MODIFIER | c.1113+3475T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89456163 | |||||||
| chr12:89456165 | C | T | 1 | a0001c0001t0004g0284 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1113+3473G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89456165 | |||||||
| chr12:89456173 | A | G | 4 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(1): Show |
4 | HG01109.hp1 HG02630.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1113+3465T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89456173 | |||||||
| chr12:89456181 | C | T | 3 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0003g0205 |
3 | HG02280.hp2 HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1113+3457G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89456181 | |||||||
| chr12:89456395 | G | A | 1 | a0001c0001t0004g0287 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1113+3243C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89456395 | |||||||
| chr12:89456520 | T | C | 4 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(1): Show |
4 | HG01109.hp1 HG02630.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1113+3118A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89456520 | |||||||
| chr12:89456541 | A | C | 1 | a0001c0001t0002g0232 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1113+3097T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89456541 | |||||||
| chr12:89456684 | A | C | 1 | a0001c0001t0001g0111 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1113+2954T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89456684 | |||||||
| chr12:89456689 | C | T | 1 | a0001c0001t0001g0092 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1113+2949G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89456689 | |||||||
| chr12:89456731 | G | T | 2 | a0001c0001t0002g0112 a0001c0001t0002g0113 |
2 | HG02132.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.1113+2907C>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89456731 | |||||||
| chr12:89456844 | T | C | 3 | a0001c0001t0002g0019 a0001c0001t0002g0152 a0001c0001t0002g0162 |
3 | HG03831.hp2 NA18954.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1113+2794A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89456844 | |||||||
| chr12:89456878 | G | A | 1 | a0001c0001t0001g0005 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1113+2760C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89456878 | |||||||
| chr12:89456898 | C | T | 4 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(1): Show |
4 | HG01109.hp1 HG02630.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1113+2740G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89456898 | |||||||
| chr12:89456918 | A | G | 1 | a0001c0001t0001g0217 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1113+2720T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89456918 | |||||||
| chr12:89457067 | C | T | 3 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0004g0284 |
3 | HG01167.hp2 HG01891.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1113+2571G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89457067 | |||||||
| chr12:89457149 | T | G | 1 | a0001c0001t0001g0012 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1113+2489A>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89457149 | |||||||
| chr12:89457189 | A | C | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(195): Show |
203 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.1113+2449T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89457189 | |||||||
| chr12:89457256 | C | T | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
195 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.1113+2382G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89457256 | |||||||
| chr12:89457317 | A | G | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
283 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.1113+2321T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89457317 | |||||||
| chr12:89457368 | T | C | 2 | a0001c0001t0001g0010 a0001c0001t0004g0040 |
2 | HG00639.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1113+2270A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89457368 | |||||||
| chr12:89457377 | A | G | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1113+2261T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89457377 | |||||||
| chr12:89457389 | C | T | 75 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0289 others(72): Show |
76 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.1113+2249G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89457389 | |||||||
| chr12:89457455 | A | C | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(277): Show |
286 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(283): Show |
intron_variant | MODIFIER | c.1113+2183T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89457455 | |||||||
| chr12:89457687 | T | C | 1 | a0001c0001t0002g0051 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1113+1951A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89457687 | |||||||
| chr12:89457799 | G | C | 1 | a0001c0001t0001g0301 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1113+1839C>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89457799 | |||||||
| chr12:89457961 | A | C | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1113+1677T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89457961 | |||||||
| chr12:89457966 | C | T | 3 | a0001c0001t0001g0245 a0001c0001t0001g0247 a0001c0001t0001g0258 |
3 | HG00733.hp2 HG01123.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1113+1672G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89457966 | |||||||
| chr12:89458044 | G | A | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1113+1594C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89458044 | |||||||
| chr12:89458130 | A | T | 1 | a0001c0001t0002g0132 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1113+1508T>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89458130 | |||||||
| chr12:89458131 | T | A | 1 | a0001c0001t0002g0132 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1113+1507A>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89458131 | |||||||
| chr12:89458144 | A | G | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
283 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.1113+1494T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89458144 | |||||||
| chr12:89458229 | G | A | 1 | a0001c0001t0002g0165 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1113+1409C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89458229 | |||||||
| chr12:89458313 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1113+1325G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89458313 | |||||||
| chr12:89458396 | G | A | 2 | a0001c0001t0002g0112 a0001c0001t0002g0113 |
2 | HG02132.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.1113+1242C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89458396 | |||||||
| chr12:89458600 | G | C | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(277): Show |
286 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(283): Show |
intron_variant | MODIFIER | c.1113+1038C>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89458600 | |||||||
| chr12:89458668 | C | T | 272 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(269): Show |
278 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(275): Show |
intron_variant | MODIFIER | c.1113+970G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89458668 | |||||||
| chr12:89458777 | G | A | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1113+861C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89458777 | |||||||
| chr12:89458812 | T | G | 1 | a0001c0001t0001g0320 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1113+826A>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89458812 | |||||||
| chr12:89458895 | A | G | 272 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(269): Show |
278 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(275): Show |
intron_variant | MODIFIER | c.1113+743T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89458895 | |||||||
| chr12:89458974 | T | C | 1 | a0001c0001t0001g0213 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1113+664A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89458974 | |||||||
| chr12:89459086 | G | C | 8 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0036 others(5): Show |
8 | HG01109.hp1 HG01167.hp2 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.1113+552C>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89459086 | |||||||
| chr12:89459149 | C | G | 6 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0003g0042 others(3): Show |
6 | HG02572.hp1 HG02615.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1113+489G>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89459149 | |||||||
| chr12:89459177 | T | G | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(195): Show |
203 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.1113+461A>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89459177 | |||||||
| chr12:89459181 | T | C | 5 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0084 others(2): Show |
5 | HG02055.hp1 HG02145.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1113+457A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89459181 | |||||||
| chr12:89459302 | C | T | 1 | a0001c0001t0001g0340 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1113+336G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89459302 | |||||||
| chr12:89459407 | TA | T | 135 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(132): Show |
137 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.1113+230delT | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89459407 | |||||||
| chr12:89459407 | TAA | T | 75 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0183 others(72): Show |
76 | HG00099.hp2 HG00597.hp2 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.1113+229_1113+230d others(4): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89459407 | |||||||
| chr12:89459529 | A | G | 4 | a0001c0001t0003g0042 a0001c0001t0005g0043 a0001c0001t0005g0044 others(1): Show |
4 | HG02615.hp1 HG03041.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1113+109T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89459529 | |||||||
| chr12:89459579 | T | G | 2 | a0001c0001t0001g0292 a0001c0001t0001g0325 |
2 | NA18951.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.1113+59A>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89459579 | |||||||
| chr12:89459610 | C | CA | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(157): Show |
164 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.1113+27dupT | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89459610 | |||||||
| chr12:89459610 | C | CAA | 29 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0025 others(26): Show |
29 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1113+26_1113+27dup others(2): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89459610 | |||||||
| chr12:89459631 | G | A | 279 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(276): Show |
285 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(282): Show |
splice_region_variant&intron_variant | LOW | c.1113+7C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 10/11 | chr12 | 89459631 | |||||||
| chr12:89459742 | T | A | 1 | a0001c0001t0001g0121 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1033-24A>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 9/11 | chr12 | 89459742 | |||||||
| chr12:89459917 | G | A | 279 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(276): Show |
285 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(282): Show |
intron_variant | MODIFIER | c.1033-199C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 9/11 | chr12 | 89459917 | |||||||
| chr12:89460232 | C | CA | 3 | a0001c0001t0006g0226 a0001c0001t0006g0227 a0001c0001t0006g0228 |
3 | HG01070.hp2 HG01361.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.1033-515dupT | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 9/11 | chr12 | 89460232 | |||||||
| chr12:89460265 | A | G | 1 | a0001c0001t0001g0046 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1033-547T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 9/11 | chr12 | 89460265 | |||||||
| chr12:89460508 | C | T | 1 | a0001c0001t0002g0021 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1033-790G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 9/11 | chr12 | 89460508 | |||||||
| chr12:89460547 | A | G | 1 | a0001c0001t0001g0027 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1033-829T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 9/11 | chr12 | 89460547 | |||||||
| chr12:89460561 | G | C | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(195): Show |
203 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.1033-843C>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 9/11 | chr12 | 89460561 | |||||||
| chr12:89460754 | A | C | 2 | a0001c0001t0001g0242 a0001c0001t0001g0246 |
2 | HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1033-1036T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 9/11 | chr12 | 89460754 | |||||||
| chr12:89461132 | TA | T | 352 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(349): Show |
358 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(355): Show |
intron_variant | MODIFIER | c.1033-1415delT | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 9/11 | chr12 | 89461132 | |||||||
| chr12:89461457 | T | C | 1 | a0001c0001t0001g0316 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1033-1739A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 9/11 | chr12 | 89461457 | |||||||
| chr12:89461490 | A | C | 2 | a0001c0001t0001g0313 a0001c0001t0001g0332 |
2 | HG02071.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1033-1772T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 9/11 | chr12 | 89461490 | |||||||
| chr12:89461937 | G | A | 1 | a0001c0001t0001g0010 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1033-2219C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 9/11 | chr12 | 89461937 | |||||||
| chr12:89462090 | C | G | 1 | a0001c0001t0001g0081 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1033-2372G>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 9/11 | chr12 | 89462090 | |||||||
| chr12:89462227 | G | C | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(194): Show |
202 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.1033-2509C>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 9/11 | chr12 | 89462227 | |||||||
| chr12:89462515 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1033-2797T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 9/11 | chr12 | 89462515 | |||||||
| chr12:89462548 | T | G | 1 | a0001c0001t0001g0161 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1033-2830A>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 9/11 | chr12 | 89462548 | |||||||
| chr12:89462687 | T | C | 1 | a0001c0001t0004g0040 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1033-2969A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 9/11 | chr12 | 89462687 | |||||||
| chr12:89463251 | A | T | 4 | a0001c0001t0002g0051 a0001c0001t0002g0114 a0001c0001t0002g0115 others(1): Show |
4 | HG02523.hp2 NA18961.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.1032+3519T>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 9/11 | chr12 | 89463251 | |||||||
| chr12:89463325 | C | T | 23 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0023 others(20): Show |
24 | HG00621.hp1 HG00733.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.1032+3445G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 9/11 | chr12 | 89463325 | |||||||
| chr12:89463347 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1032+3423G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 9/11 | chr12 | 89463347 | |||||||
| chr12:89463361 | G | A | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(277): Show |
286 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(283): Show |
intron_variant | MODIFIER | c.1032+3409C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 9/11 | chr12 | 89463361 | |||||||
| chr12:89463427 | T | TCA | 109 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0027 others(106): Show |
111 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.1032+3341_1032+334 others(6): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 9/11 | chr12 | 89463427 | |||||||
| chr12:89463646 | A | C | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(270): Show |
279 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(276): Show |
intron_variant | MODIFIER | c.1032+3124T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 9/11 | chr12 | 89463646 | |||||||
| chr12:89463703 | G | A | 2 | a0001c0001t0002g0112 a0001c0001t0002g0113 |
2 | HG02132.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.1032+3067C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 9/11 | chr12 | 89463703 | |||||||
| chr12:89463801 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1032+2969G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 9/11 | chr12 | 89463801 | |||||||
| chr12:89463834 | C | T | 76 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0289 others(73): Show |
77 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1032+2936G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 9/11 | chr12 | 89463834 | |||||||
| chr12:89464147 | T | C | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(62): Show |
68 | HG00423.hp2 HG00673.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.1032+2623A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 9/11 | chr12 | 89464147 | |||||||
| chr12:89464164 | G | T | 1 | a0001c0001t0001g0076 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1032+2606C>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 9/11 | chr12 | 89464164 | |||||||
| chr12:89464238 | AC | A | 3 | a0001c0001t0001g0052 a0001c0001t0001g0070 a0001c0001t0001g0075 |
3 | HG00735.hp1 HG01952.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1032+2531delG | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 9/11 | chr12 | 89464238 | |||||||
| chr12:89464425 | A | G | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1032+2345T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 9/11 | chr12 | 89464425 | |||||||
| chr12:89464483 | G | GT | 75 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0034 others(72): Show |
76 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.1032+2286dupA | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 9/11 | chr12 | 89464483 | |||||||
| chr12:89464483 | G | GTT | 30 | a0001c0001t0001g0011 a0001c0001t0001g0025 a0001c0001t0001g0026 others(27): Show |
30 | HG00099.hp1 HG01106.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.1032+2285_1032+228 others(6): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 9/11 | chr12 | 89464483 | |||||||
| chr12:89464483 | G | GTTT | 131 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(128): Show |
134 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(131): Show |
intron_variant | MODIFIER | c.1032+2284_1032+228 others(7): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 9/11 | chr12 | 89464483 | |||||||
| chr12:89464483 | G | GTTTT | 39 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(36): Show |
41 | HG00423.hp1 HG00423.hp2 HG01175.hp1 others(38): Show |
intron_variant | MODIFIER | c.1032+2283_1032+228 others(8): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 9/11 | chr12 | 89464483 | |||||||
| chr12:89464483 | GT | G | 8 | a0001c0001t0001g0233 a0001c0001t0001g0242 a0001c0001t0001g0246 others(5): Show |
8 | HG01070.hp2 HG01361.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1032+2286delA | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 9/11 | chr12 | 89464483 | |||||||
| chr12:89464483 | GTTTT | G | 6 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0183 others(3): Show |
6 | HG02135.hp1 NA18944.hp2 NA19007.hp1 others(3): Show |
intron_variant | MODIFIER | c.1032+2283_1032+228 others(8): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 9/11 | chr12 | 89464483 | |||||||
| chr12:89464719 | A | C | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(270): Show |
279 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(276): Show |
intron_variant | MODIFIER | c.1032+2051T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 9/11 | chr12 | 89464719 | |||||||
| chr12:89464802 | G | GA | 78 | a0001c0001t0001g0007 a0001c0001t0001g0030 a0001c0001t0001g0034 others(75): Show |
79 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.1032+1967dupT | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 9/11 | chr12 | 89464802 | |||||||
| chr12:89464802 | GA | G | 25 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0039 others(22): Show |
25 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.1032+1967delT | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 9/11 | chr12 | 89464802 | |||||||
| chr12:89464977 | G | A | 2 | a0001c0001t0001g0237 a0001c0001t0001g0253 |
2 | HG01517.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1032+1793C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 9/11 | chr12 | 89464977 | |||||||
| chr12:89465062 | G | A | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(62): Show |
68 | HG00423.hp2 HG00673.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.1032+1708C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 9/11 | chr12 | 89465062 | |||||||
| chr12:89465312 | T | C | 1 | a0001c0001t0001g0010 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1032+1458A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 9/11 | chr12 | 89465312 | |||||||
| chr12:89465369 | C | T | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1032+1401G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 9/11 | chr12 | 89465369 | |||||||
| chr12:89465831 | C | G | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(186): Show |
194 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.1032+939G>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 9/11 | chr12 | 89465831 | |||||||
| chr12:89465901 | G | A | 5 | a0001c0001t0002g0124 a0001c0001t0002g0156 a0001c0001t0002g0157 others(2): Show |
5 | HG01081.hp2 HG01928.hp1 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.1032+869C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 9/11 | chr12 | 89465901 | |||||||
| chr12:89466241 | G | T | 2 | a0001c0001t0001g0229 a0001c0004t0001g0264 |
2 | HG03130.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1032+529C>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 9/11 | chr12 | 89466241 | |||||||
| chr12:89466515 | A | C | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1032+255T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 9/11 | chr12 | 89466515 | |||||||
| chr12:89466542 | C | A | 76 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0289 others(73): Show |
77 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1032+228G>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 9/11 | chr12 | 89466542 | |||||||
| chr12:89467156 | T | C | 1 | a0001c0001t0001g0010 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.880-234A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 8/11 | chr12 | 89467156 | |||||||
| chr12:89467377 | G | A | 2 | a0001c0001t0001g0336 a0001c0001t0001g0343 |
2 | HG01517.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.879+240C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 8/11 | chr12 | 89467377 | |||||||
| chr12:89467488 | C | G | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(270): Show |
279 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(276): Show |
intron_variant | MODIFIER | c.879+129G>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 8/11 | chr12 | 89467488 | |||||||
| chr12:89467752 | T | C | 76 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0289 others(73): Show |
77 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.811-67A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 7/11 | chr12 | 89467752 | |||||||
| chr12:89468069 | C | T | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.811-384G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 7/11 | chr12 | 89468069 | |||||||
| chr12:89468189 | G | T | 1 | a0001c0001t0001g0017 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.811-504C>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 7/11 | chr12 | 89468189 | |||||||
| chr12:89468253 | G | T | 76 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0289 others(73): Show |
77 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.811-568C>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 7/11 | chr12 | 89468253 | |||||||
| chr12:89468264 | C | A | 4 | a0001c0001t0003g0042 a0001c0001t0005g0043 a0001c0001t0005g0044 others(1): Show |
4 | HG02615.hp1 HG03041.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.811-579G>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 7/11 | chr12 | 89468264 | |||||||
| chr12:89468317 | C | T | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.811-632G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 7/11 | chr12 | 89468317 | |||||||
| chr12:89468596 | G | A | 3 | a0001c0001t0001g0200 a0001c0001t0001g0202 a0001c0001t0001g0203 |
3 | HG00642.hp2 HG02004.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.811-911C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 7/11 | chr12 | 89468596 | |||||||
| chr12:89468675 | TTA | T | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(194): Show |
202 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.811-992_811-991del others(2): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 7/11 | chr12 | 89468675 | |||||||
| chr12:89468727 | T | A | 1 | a0001c0001t0001g0221 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.811-1042A>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 7/11 | chr12 | 89468727 | |||||||
| chr12:89468835 | C | T | 1 | a0001c0001t0001g0010 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.811-1150G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 7/11 | chr12 | 89468835 | |||||||
| chr12:89468887 | CA | C | 275 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(272): Show |
281 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(278): Show |
intron_variant | MODIFIER | c.811-1203delT | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 7/11 | chr12 | 89468887 | |||||||
| chr12:89468936 | T | G | 1 | a0001c0001t0001g0312 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.811-1251A>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 7/11 | chr12 | 89468936 | |||||||
| chr12:89469052 | G | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0037 |
2 | HG02976.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.810+1309C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 7/11 | chr12 | 89469052 | |||||||
| chr12:89469070 | G | T | 1 | a0001c0001t0008g0360 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.810+1291C>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 7/11 | chr12 | 89469070 | |||||||
| chr12:89469102 | T | TAAAC | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.810+1255_810+1258d others(6): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 7/11 | chr12 | 89469102 | |||||||
| chr12:89469177 | T | C | 1 | a0001c0001t0001g0343 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.810+1184A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 7/11 | chr12 | 89469177 | |||||||
| chr12:89469348 | C | T | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.810+1013G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 7/11 | chr12 | 89469348 | |||||||
| chr12:89469396 | A | C | 1 | a0001c0001t0001g0108 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.810+965T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 7/11 | chr12 | 89469396 | |||||||
| chr12:89469576 | C | T | 6 | a0001c0001t0001g0031 a0001c0001t0001g0237 a0001c0001t0001g0251 others(3): Show |
6 | HG01074.hp1 HG01099.hp1 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.810+785G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 7/11 | chr12 | 89469576 | |||||||
| chr12:89469689 | C | T | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.810+672G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 7/11 | chr12 | 89469689 | |||||||
| chr12:89469695 | G | A | 3 | a0001c0001t0006g0226 a0001c0001t0006g0227 a0001c0001t0006g0228 |
3 | HG01070.hp2 HG01361.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.810+666C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 7/11 | chr12 | 89469695 | |||||||
| chr12:89469878 | AT | A | 274 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(271): Show |
280 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(277): Show |
intron_variant | MODIFIER | c.810+482delA | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 7/11 | chr12 | 89469878 | |||||||
| chr12:89469928 | T | C | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(270): Show |
279 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(276): Show |
intron_variant | MODIFIER | c.810+433A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 7/11 | chr12 | 89469928 | |||||||
| chr12:89469974 | G | A | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.810+387C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 7/11 | chr12 | 89469974 | |||||||
| chr12:89470082 | A | T | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.810+279T>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 7/11 | chr12 | 89470082 | |||||||
| chr12:89470179 | A | G | 1 | a0001c0001t0002g0307 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.810+182T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 7/11 | chr12 | 89470179 | |||||||
| chr12:89470270 | C | T | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
283 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.810+91G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 7/11 | chr12 | 89470270 | |||||||
| chr12:89470320 | A | G | 1 | a0001c0001t0001g0110 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.810+41T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 7/11 | chr12 | 89470320 | |||||||
| chr12:89470655 | T | A | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
283 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.677-161A>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 6/11 | chr12 | 89470655 | |||||||
| chr12:89470660 | G | A | 3 | a0001c0001t0006g0226 a0001c0001t0006g0227 a0001c0001t0006g0228 |
3 | HG01070.hp2 HG01361.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.677-166C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 6/11 | chr12 | 89470660 | |||||||
| chr12:89470676 | C | T | 1 | a0001c0001t0001g0283 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.677-182G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 6/11 | chr12 | 89470676 | |||||||
| chr12:89470708 | G | A | 1 | a0001c0001t0001g0016 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.677-214C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 6/11 | chr12 | 89470708 | |||||||
| chr12:89470719 | C | A | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.677-225G>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 6/11 | chr12 | 89470719 | |||||||
| chr12:89470865 | G | A | 89 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0023 others(86): Show |
90 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.677-371C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 6/11 | chr12 | 89470865 | |||||||
| chr12:89471015 | T | C | 3 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 |
3 | HG01192.hp1 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.677-521A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 6/11 | chr12 | 89471015 | |||||||
| chr12:89471042 | T | C | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.677-548A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 6/11 | chr12 | 89471042 | |||||||
| chr12:89471050 | T | C | 6 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0003g0042 others(3): Show |
6 | HG02572.hp1 HG02615.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.677-556A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 6/11 | chr12 | 89471050 | |||||||
| chr12:89471149 | A | G | 3 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0004g0284 |
3 | HG01167.hp2 HG01891.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.676+465T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 6/11 | chr12 | 89471149 | |||||||
| chr12:89471173 | C | T | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.676+441G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 6/11 | chr12 | 89471173 | |||||||
| chr12:89471385 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.676+229A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 6/11 | chr12 | 89471385 | |||||||
| chr12:89471768 | C | CT | 7 | a0001c0001t0001g0004 a0001c0001t0001g0104 a0001c0001t0001g0105 others(4): Show |
8 | HG01261.hp2 HG02486.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.561-40dupA | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 5/11 | chr12 | 89471768 | |||||||
| chr12:89471768 | C | CTTT | 71 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0289 others(68): Show |
72 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.561-42_561-40dupAA others(1): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 5/11 | chr12 | 89471768 | |||||||
| chr12:89471789 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.561-60G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 5/11 | chr12 | 89471789 | |||||||
| chr12:89471790 | G | A | 1 | a0001c0001t0001g0286 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.561-61C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 5/11 | chr12 | 89471790 | |||||||
| chr12:89471810 | CAGGCTGG others(3): Show |
C | 1 | a0001c0001t0001g0168 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.561-91_561-82delAC others(8): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 5/11 | chr12 | 89471810 | |||||||
| chr12:89471892 | C | T | 1 | a0001c0001t0003g0351 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.561-163G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 5/11 | chr12 | 89471892 | |||||||
| chr12:89471915 | A | G | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG01167.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.561-186T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 5/11 | chr12 | 89471915 | |||||||
| chr12:89471969 | T | C | 1 | a0001c0001t0001g0011 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.560+199A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 5/11 | chr12 | 89471969 | |||||||
| chr12:89472009 | C | T | 3 | a0001c0001t0006g0226 a0001c0001t0006g0227 a0001c0001t0006g0228 |
3 | HG01070.hp2 HG01361.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.560+159G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 5/11 | chr12 | 89472009 | |||||||
| chr12:89472118 | G | A | 1 | a0001c0001t0001g0265 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.560+50C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 5/11 | chr12 | 89472118 | |||||||
| chr12:89472277 | TAGAAAGA others(3): Show |
T | 200 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(197): Show |
205 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(202): Show |
splice_region_variant&intron_variant | LOW | c.453-12_453-3delTCT others(7): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89472277 | |||||||
| chr12:89472483 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.453-208A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89472483 | |||||||
| chr12:89472652 | G | A | 1 | a0001c0001t0001g0062 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.453-377C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89472652 | |||||||
| chr12:89472702 | T | G | 1 | a0001c0001t0001g0268 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.453-427A>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89472702 | |||||||
| chr12:89473003 | A | G | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(62): Show |
68 | HG00423.hp2 HG00673.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.453-728T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89473003 | |||||||
| chr12:89473178 | C | G | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.453-903G>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89473178 | |||||||
| chr12:89473655 | G | A | 6 | a0001c0001t0001g0300 a0001c0001t0001g0302 a0001c0001t0001g0320 others(3): Show |
6 | HG02280.hp1 HG02615.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.453-1380C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89473655 | |||||||
| chr12:89473666 | G | GA | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
257 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(254): Show |
intron_variant | MODIFIER | c.453-1392dupT | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89473666 | |||||||
| chr12:89473666 | G | GAA | 16 | a0001c0001t0001g0068 a0001c0001t0001g0111 a0001c0001t0001g0299 others(13): Show |
16 | HG00323.hp2 HG00738.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.453-1393_453-1392d others(4): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89473666 | |||||||
| chr12:89473687 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.453-1412C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89473687 | |||||||
| chr12:89473688 | T | G | 1 | a0001c0001t0001g0066 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.453-1413A>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89473688 | |||||||
| chr12:89473738 | C | T | 1 | a0001c0001t0001g0110 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.453-1463G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89473738 | |||||||
| chr12:89473782 | A | G | 1 | a0002c0003t0001g0288 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.453-1507T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89473782 | |||||||
| chr12:89473890 | C | T | 2 | a0001c0001t0001g0337 a0001c0001t0001g0341 |
2 | HG01081.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.453-1615G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89473890 | |||||||
| chr12:89473970 | C | T | 18 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0192 others(15): Show |
18 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.453-1695G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89473970 | |||||||
| chr12:89474077 | G | A | 1 | a0001c0001t0001g0010 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.453-1802C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89474077 | |||||||
| chr12:89474107 | G | A | 1 | a0001c0001t0002g0020 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.453-1832C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89474107 | |||||||
| chr12:89474175 | T | C | 2 | a0001c0001t0001g0313 a0001c0001t0001g0332 |
2 | HG02071.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.453-1900A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89474175 | |||||||
| chr12:89474314 | CA | C | 26 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0023 others(23): Show |
27 | HG00621.hp1 HG00733.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.453-2040delT | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89474314 | |||||||
| chr12:89474386 | A | G | 1 | a0001c0001t0001g0230 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.453-2111T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89474386 | |||||||
| chr12:89474394 | C | T | 2 | a0001c0001t0001g0336 a0001c0001t0001g0343 |
2 | HG01517.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.453-2119G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89474394 | |||||||
| chr12:89474506 | G | A | 3 | a0001c0001t0007g0033 a0001c0001t0007g0277 a0001c0001t0007g0278 |
3 | NA18959.hp1 NA18989.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.453-2231C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89474506 | |||||||
| chr12:89474759 | G | C | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | HG01346.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.453-2484C>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89474759 | |||||||
| chr12:89474870 | C | G | 1 | a0001c0001t0001g0110 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.453-2595G>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89474870 | |||||||
| chr12:89474973 | A | G | 6 | a0001c0001t0001g0031 a0001c0001t0001g0237 a0001c0001t0001g0251 others(3): Show |
6 | HG01074.hp1 HG01099.hp1 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.453-2698T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89474973 | |||||||
| chr12:89475119 | G | T | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.453-2844C>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89475119 | |||||||
| chr12:89475290 | T | C | 1 | a0001c0001t0001g0016 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.453-3015A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89475290 | |||||||
| chr12:89475547 | A | G | 19 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0191 others(16): Show |
19 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.453-3272T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89475547 | |||||||
| chr12:89475820 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.453-3545G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89475820 | |||||||
| chr12:89475840 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.453-3565C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89475840 | |||||||
| chr12:89475894 | A | G | 1 | a0001c0001t0001g0068 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.453-3619T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89475894 | |||||||
| chr12:89475910 | C | CT | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(98): Show |
104 | HG00099.hp1 HG00423.hp2 HG00639.hp2 others(101): Show |
intron_variant | MODIFIER | c.453-3636dupA | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89475910 | |||||||
| chr12:89475910 | C | CTT | 74 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0025 others(71): Show |
75 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.453-3637_453-3636d others(4): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89475910 | |||||||
| chr12:89475910 | C | CTTT | 28 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0023 others(25): Show |
29 | HG00621.hp1 HG00733.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.453-3638_453-3636d others(5): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89475910 | |||||||
| chr12:89475910 | CT | C | 10 | a0001c0001t0001g0210 a0001c0001t0001g0248 a0001c0001t0001g0266 others(7): Show |
10 | HG00558.hp2 HG01943.hp2 HG02165.hp2 others(7): Show |
intron_variant | MODIFIER | c.453-3636delA | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89475910 | |||||||
| chr12:89476068 | G | A | 1 | a0001c0001t0001g0223 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.453-3793C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89476068 | |||||||
| chr12:89476091 | G | C | 1 | a0001c0001t0001g0249 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.453-3816C>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89476091 | |||||||
| chr12:89476187 | A | G | 354 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(351): Show |
361 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(358): Show |
intron_variant | MODIFIER | c.453-3912T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89476187 | |||||||
| chr12:89476432 | C | T | 3 | a0001c0001t0006g0226 a0001c0001t0006g0227 a0001c0001t0006g0228 |
3 | HG01070.hp2 HG01361.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.453-4157G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89476432 | |||||||
| chr12:89476492 | G | A | 2 | a0001c0001t0001g0242 a0001c0001t0001g0246 |
2 | HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.453-4217C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89476492 | |||||||
| chr12:89476653 | C | T | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.453-4378G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89476653 | |||||||
| chr12:89476697 | A | AATAG | 7 | a0001c0001t0001g0028 a0001c0001t0001g0039 a0001c0001t0001g0063 others(4): Show |
7 | HG02572.hp1 HG02572.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.453-4426_453-4423d others(6): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89476697 | |||||||
| chr12:89476697 | A | AATAGATA others(5): Show |
1 | a0001c0001t0004g0284 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.453-4434_453-4423d others(14): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89476697 | |||||||
| chr12:89476697 | AATAG | A | 38 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0109 others(35): Show |
38 | HG00323.hp2 HG00558.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.453-4426_453-4423d others(6): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89476697 | |||||||
| chr12:89476697 | AATAGATA others(1): Show |
A | 23 | a0001c0001t0001g0108 a0001c0001t0001g0229 a0001c0001t0001g0231 others(20): Show |
23 | HG00323.hp1 HG00597.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.453-4430_453-4423d others(10): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89476697 | |||||||
| chr12:89476697 | AATAGATA others(5): Show |
A | 22 | a0001c0001t0001g0031 a0001c0001t0001g0046 a0001c0001t0001g0050 others(19): Show |
22 | HG00735.hp2 HG01074.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.453-4434_453-4423d others(14): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89476697 | |||||||
| chr12:89476697 | AATAGATA others(9): Show |
A | 1 | a0001c0001t0001g0301 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.453-4438_453-4423d others(18): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89476697 | |||||||
| chr12:89476697 | AATAGATA others(13): Show |
A | 1 | a0001c0001t0001g0255 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.453-4442_453-4423d others(22): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89476697 | |||||||
| chr12:89476697 | AATAGATA others(17): Show |
A | 1 | a0001c0001t0001g0034 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.453-4446_453-4423d others(26): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89476697 | |||||||
| chr12:89476723 | TAGATAGA others(33): Show |
T | 1 | a0001c0001t0002g0021 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.453-4488_453-4449d others(42): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89476723 | |||||||
| chr12:89476727 | TAGATAGA others(29): Show |
T | 1 | a0001c0001t0002g0165 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.453-4488_453-4453d others(38): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89476727 | |||||||
| chr12:89476735 | T | TAGATAGA others(49): Show |
1 | a0001c0001t0001g0035 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.453-4461_453-4460i others(58): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89476735 | |||||||
| chr12:89476735 | TAGATAGA others(21): Show |
T | 54 | a0001c0001t0001g0103 a0001c0001t0001g0110 a0001c0001t0001g0111 others(51): Show |
54 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.453-4488_453-4461d others(30): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89476735 | |||||||
| chr12:89476739 | T | TAGATAGA others(45): Show |
1 | a0001c0001t0001g0038 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.453-4465_453-4464i others(54): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89476739 | |||||||
| chr12:89476739 | T | TAGATAGA others(65): Show |
1 | a0001c0001t0001g0037 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.453-4465_453-4464i others(74): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89476739 | |||||||
| chr12:89476739 | TAGATAGA others(17): Show |
T | 28 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0170 others(25): Show |
28 | HG00621.hp1 HG00733.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.453-4488_453-4465d others(26): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89476739 | |||||||
| chr12:89476743 | T | TAGATAGA others(13): Show |
1 | a0001c0001t0001g0011 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.453-4469_453-4468i others(22): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89476743 | |||||||
| chr12:89476743 | T | TAGATAGA others(49): Show |
1 | a0001c0001t0001g0036 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.453-4469_453-4468i others(58): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89476743 | |||||||
| chr12:89476743 | TAGATAGA others(13): Show |
T | 7 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0117 others(4): Show |
8 | HG02027.hp1 HG03239.hp1 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.453-4488_453-4469d others(22): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89476743 | |||||||
| chr12:89476747 | TAGATAGA others(9): Show |
T | 15 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(12): Show |
15 | HG00642.hp2 HG00673.hp2 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.453-4488_453-4473d others(18): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89476747 | |||||||
| chr12:89476747 | TAGATAGA others(13): Show |
T | 4 | a0001c0001t0001g0078 a0001c0001t0006g0226 a0001c0001t0006g0227 others(1): Show |
4 | HG01070.hp2 HG01361.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.453-4492_453-4473d others(22): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89476747 | |||||||
| chr12:89476751 | TAGATAGA others(5): Show |
T | 53 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(50): Show |
54 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.453-4488_453-4477d others(14): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89476751 | |||||||
| chr12:89476751 | TAGATAGA others(9): Show |
T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0055 a0001c0001t0004g0040 |
3 | HG00639.hp1 HG02559.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.453-4492_453-4477d others(18): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89476751 | |||||||
| chr12:89476755 | T | C | 1 | a0001c0001t0001g0011 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.453-4480A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89476755 | |||||||
| chr12:89476755 | TAGATAGA others(1): Show |
T | 19 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(16): Show |
20 | HG00741.hp2 HG01257.hp1 HG01258.hp2 others(17): Show |
intron_variant | MODIFIER | c.453-4488_453-4481d others(10): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89476755 | |||||||
| chr12:89476755 | TAGATAGA others(5): Show |
T | 3 | a0001c0001t0001g0107 a0001c0001t0008g0359 a0001c0001t0008g0361 |
3 | HG02622.hp2 HG02717.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.453-4492_453-4481d others(14): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89476755 | |||||||
| chr12:89476759 | T | C | 9 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0246 others(6): Show |
9 | HG01081.hp1 HG01123.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.453-4484A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89476759 | |||||||
| chr12:89476759 | T | TAGATAGA others(5): Show |
5 | a0001c0001t0001g0223 a0001c0001t0001g0230 a0001c0001t0001g0256 others(2): Show |
5 | HG02080.hp2 HG02083.hp2 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.453-4485_453-4484i others(14): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89476759 | |||||||
| chr12:89476759 | T | TAGATAGA others(9): Show |
4 | a0001c0001t0001g0029 a0001c0001t0001g0224 a0001c0001t0001g0240 others(1): Show |
4 | NA18612.hp1 NA18990.hp2 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.453-4485_453-4484i others(18): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89476759 | |||||||
| chr12:89476759 | T | TAGATAGA others(17): Show |
1 | a0001c0001t0001g0236 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.453-4485_453-4484i others(26): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89476759 | |||||||
| chr12:89476759 | T | TAGATAGA others(21): Show |
1 | a0001c0001t0001g0006 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.453-4485_453-4484i others(30): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89476759 | |||||||
| chr12:89476759 | T | TAGATAGA others(25): Show |
1 | a0001c0001t0001g0006 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.453-4485_453-4484i others(34): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89476759 | |||||||
| chr12:89476759 | T | TAGATAGA others(29): Show |
1 | a0001c0001t0001g0216 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.453-4485_453-4484i others(38): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89476759 | |||||||
| chr12:89476759 | T | TAGATAGA others(33): Show |
2 | a0001c0001t0001g0215 a0001c0001t0001g0217 |
2 | HG00673.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.453-4485_453-4484i others(42): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89476759 | |||||||
| chr12:89476759 | T | TAGATAGA others(45): Show |
1 | a0001c0001t0001g0027 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.453-4485_453-4484i others(54): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89476759 | |||||||
| chr12:89476759 | T | TAGATAGA others(33): Show |
2 | a0001c0001t0001g0214 a0001c0001t0001g0220 |
2 | HG02809.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.453-4485_453-4484i others(42): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89476759 | |||||||
| chr12:89476759 | T | TAGATAGA others(37): Show |
1 | a0001c0001t0001g0219 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.453-4485_453-4484i others(46): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89476759 | |||||||
| chr12:89476759 | T | TAGATAGA others(37): Show |
1 | a0001c0001t0001g0225 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.453-4485_453-4484i others(46): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89476759 | |||||||
| chr12:89476759 | T | TAGATAGA others(49): Show |
1 | a0001c0001t0001g0218 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.453-4485_453-4484i others(58): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89476759 | |||||||
| chr12:89476759 | TAGAC | T | 24 | a0001c0001t0001g0014 a0001c0001t0001g0048 a0001c0001t0001g0059 others(21): Show |
24 | HG00423.hp2 HG00738.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.453-4488_453-4485d others(6): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89476759 | |||||||
| chr12:89476759 | TAGACAGA others(1): Show |
T | 3 | a0001c0001t0001g0004 a0001c0001t0012g0106 a0001c0001t0015g0358 |
4 | HG02486.hp1 HG02723.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.453-4492_453-4485d others(10): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89476759 | |||||||
| chr12:89476763 | C | T | 11 | a0001c0001t0001g0012 a0001c0001t0001g0061 a0001c0001t0001g0063 others(8): Show |
11 | HG00099.hp2 HG02145.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.453-4488G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89476763 | |||||||
| chr12:89476767 | C | T | 4 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0191 others(1): Show |
4 | HG02809.hp2 HG02886.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.453-4492G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89476767 | |||||||
| chr12:89476774 | A | G | 3 | a0001c0001t0001g0069 a0001c0001t0001g0071 a0001c0001t0001g0077 |
3 | NA18942.hp1 NA18980.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.453-4499T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89476774 | |||||||
| chr12:89476954 | A | G | 2 | a0001c0001t0002g0154 a0001c0001t0002g0155 |
2 | NA19056.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.453-4679T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89476954 | |||||||
| chr12:89477008 | C | T | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(277): Show |
286 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(283): Show |
intron_variant | MODIFIER | c.453-4733G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89477008 | |||||||
| chr12:89477011 | GTCCTGAA others(13): Show |
G | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.453-4756_453-4737d others(22): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89477011 | |||||||
| chr12:89477188 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.453-4913A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89477188 | |||||||
| chr12:89477403 | A | C | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(277): Show |
286 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(283): Show |
intron_variant | MODIFIER | c.453-5128T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89477403 | |||||||
| chr12:89477409 | T | C | 6 | a0001c0001t0001g0031 a0001c0001t0001g0237 a0001c0001t0001g0251 others(3): Show |
6 | HG01074.hp1 HG01099.hp1 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.453-5134A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89477409 | |||||||
| chr12:89477640 | T | A | 1 | a0001c0001t0001g0317 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.453-5365A>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89477640 | |||||||
| chr12:89477698 | T | C | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.453-5423A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89477698 | |||||||
| chr12:89477716 | G | T | 18 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0192 others(15): Show |
18 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.453-5441C>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89477716 | |||||||
| chr12:89477836 | G | A | 75 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0289 others(72): Show |
76 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.453-5561C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89477836 | |||||||
| chr12:89478077 | A | ACATT | 4 | a0001c0001t0001g0034 a0001c0001t0001g0306 a0001c0001t0001g0342 others(1): Show |
4 | HG00738.hp2 HG01891.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.453-5806_453-5803d others(6): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89478077 | |||||||
| chr12:89478077 | ACATT | A | 53 | a0001c0001t0001g0024 a0001c0001t0001g0030 a0001c0001t0001g0046 others(50): Show |
53 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.453-5806_453-5803d others(6): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89478077 | |||||||
| chr12:89478077 | ACATTCAT others(1): Show |
A | 126 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0022 others(123): Show |
128 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.453-5810_453-5803d others(10): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89478077 | |||||||
| chr12:89478077 | ACATTCAT others(5): Show |
A | 102 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(99): Show |
106 | HG00099.hp1 HG00423.hp2 HG00639.hp2 others(103): Show |
intron_variant | MODIFIER | c.453-5814_453-5803d others(14): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89478077 | |||||||
| chr12:89478077 | ACATTCAT others(9): Show |
A | 5 | a0001c0001t0004g0284 a0001c0001t0008g0359 a0001c0001t0008g0360 others(2): Show |
5 | HG01891.hp1 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.453-5818_453-5803d others(18): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89478077 | |||||||
| chr12:89478077 | ACATTCAT others(13): Show |
A | 2 | a0001c0001t0001g0016 a0001c0001t0005g0043 |
2 | HG02080.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.453-5822_453-5803d others(22): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89478077 | |||||||
| chr12:89478110 | CATTCATT others(9): Show |
C | 1 | a0001c0001t0004g0040 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.453-5851_453-5836d others(18): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89478110 | |||||||
| chr12:89478162 | T | C | 1 | a0001c0001t0001g0097 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.453-5887A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89478162 | |||||||
| chr12:89478170 | C | T | 4 | a0001c0001t0001g0352 a0001c0001t0003g0350 a0001c0001t0003g0351 others(1): Show |
4 | HG02647.hp1 HG02922.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.453-5895G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89478170 | |||||||
| chr12:89478365 | C | T | 6 | a0001c0001t0001g0004 a0001c0001t0001g0104 a0001c0001t0001g0105 others(3): Show |
7 | HG02486.hp1 HG02723.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.453-6090G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89478365 | |||||||
| chr12:89478399 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.453-6124C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89478399 | |||||||
| chr12:89478414 | TG | T | 3 | a0001c0001t0001g0289 a0001c0001t0001g0293 a0001c0001t0001g0294 |
3 | HG02602.hp2 HG03239.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.453-6140delC | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89478414 | |||||||
| chr12:89478602 | CTT | C | 6 | a0001c0001t0001g0300 a0001c0001t0001g0302 a0001c0001t0001g0320 others(3): Show |
6 | HG02280.hp1 HG02615.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.453-6329_453-6328d others(4): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89478602 | |||||||
| chr12:89478671 | T | C | 3 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0004g0284 |
3 | HG01167.hp2 HG01891.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.453-6396A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89478671 | |||||||
| chr12:89478729 | T | C | 6 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(3): Show |
6 | HG00673.hp1 HG02165.hp1 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.453-6454A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89478729 | |||||||
| chr12:89478771 | G | A | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | HG01346.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.453-6496C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89478771 | |||||||
| chr12:89479004 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.453-6729T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89479004 | |||||||
| chr12:89479155 | C | T | 76 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0123 others(73): Show |
77 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.453-6880G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89479155 | |||||||
| chr12:89479372 | C | G | 1 | a0001c0001t0004g0284 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.453-7097G>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89479372 | |||||||
| chr12:89479561 | A | C | 12 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0192 others(9): Show |
12 | HG00099.hp1 HG00639.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.453-7286T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89479561 | |||||||
| chr12:89479572 | GTTAAA | G | 64 | a0001c0001t0001g0103 a0001c0001t0001g0110 a0001c0001t0001g0111 others(61): Show |
64 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.453-7302_453-7298d others(7): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89479572 | |||||||
| chr12:89479589 | C | T | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(62): Show |
68 | HG00423.hp2 HG00673.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.453-7314G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89479589 | |||||||
| chr12:89479639 | G | A | 1 | a0001c0001t0001g0223 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.453-7364C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89479639 | |||||||
| chr12:89480142 | G | GT | 82 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0025 others(79): Show |
83 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.453-7868dupA | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89480142 | |||||||
| chr12:89480198 | A | T | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(199): Show |
207 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(204): Show |
intron_variant | MODIFIER | c.453-7923T>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89480198 | |||||||
| chr12:89480348 | G | A | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(62): Show |
68 | HG00423.hp2 HG00673.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.453-8073C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89480348 | |||||||
| chr12:89480442 | T | A | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.453-8167A>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89480442 | |||||||
| chr12:89480489 | C | T | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.453-8214G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89480489 | |||||||
| chr12:89480595 | A | AT | 6 | a0001c0001t0001g0028 a0001c0001t0001g0127 a0001c0001t0001g0255 others(3): Show |
6 | HG02572.hp2 HG04115.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.453-8321dupA | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89480595 | |||||||
| chr12:89480595 | AT | A | 110 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0022 others(107): Show |
112 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.453-8321delA | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89480595 | |||||||
| chr12:89480595 | ATT | A | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(98): Show |
104 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(101): Show |
intron_variant | MODIFIER | c.453-8322_453-8321d others(4): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89480595 | |||||||
| chr12:89480666 | C | T | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.453-8391G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89480666 | |||||||
| chr12:89480802 | A | G | 19 | a0001c0001t0001g0034 a0001c0001t0001g0120 a0001c0001t0001g0122 others(16): Show |
19 | HG03710.hp1 HG04115.hp1 NA18939.hp2 others(16): Show |
intron_variant | MODIFIER | c.453-8527T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89480802 | |||||||
| chr12:89480880 | A | G | 1 | a0001c0001t0001g0180 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.453-8605T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89480880 | |||||||
| chr12:89481039 | CAGGGCCT others(7): Show |
C | 70 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(67): Show |
73 | HG00423.hp2 HG00673.hp2 HG00735.hp1 others(70): Show |
intron_variant | MODIFIER | c.453-8778_453-8765d others(16): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89481039 | |||||||
| chr12:89481522 | C | T | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.453-9247G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89481522 | |||||||
| chr12:89481563 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.453-9288C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89481563 | |||||||
| chr12:89481583 | G | A | 3 | a0001c0001t0001g0354 a0001c0001t0001g0356 a0001c0001t0001g0357 |
3 | HG00099.hp2 HG03491.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.453-9308C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89481583 | |||||||
| chr12:89481613 | A | C | 1 | a0001c0001t0002g0119 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.453-9338T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89481613 | |||||||
| chr12:89481802 | C | G | 16 | a0001c0001t0001g0116 a0001c0001t0002g0019 a0001c0001t0002g0020 others(13): Show |
16 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(13): Show |
intron_variant | MODIFIER | c.453-9527G>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89481802 | |||||||
| chr12:89481887 | A | G | 3 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 |
3 | HG01192.hp1 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.453-9612T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89481887 | |||||||
| chr12:89481900 | C | T | 7 | a0001c0001t0001g0337 a0001c0001t0001g0338 a0001c0001t0001g0339 others(4): Show |
7 | HG00323.hp2 HG00738.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.453-9625G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89481900 | |||||||
| chr12:89481901 | C | T | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.453-9626G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89481901 | |||||||
| chr12:89481912 | A | G | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(62): Show |
68 | HG00423.hp2 HG00673.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.453-9637T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89481912 | |||||||
| chr12:89482017 | A | G | 1 | a0001c0001t0001g0220 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.453-9742T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89482017 | |||||||
| chr12:89482366 | T | C | 75 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0289 others(72): Show |
76 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.452+9570A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89482366 | |||||||
| chr12:89482427 | G | A | 1 | a0001c0001t0001g0357 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.452+9509C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89482427 | |||||||
| chr12:89482708 | C | A | 1 | a0001c0001t0001g0321 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.452+9228G>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89482708 | |||||||
| chr12:89482932 | T | A | 1 | a0002c0003t0001g0288 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.452+9004A>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89482932 | |||||||
| chr12:89483146 | C | T | 75 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0289 others(72): Show |
76 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.452+8790G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89483146 | |||||||
| chr12:89483504 | G | A | 3 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 |
3 | HG01192.hp1 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.452+8432C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89483504 | |||||||
| chr12:89483586 | C | A | 3 | a0001c0001t0001g0007 a0001c0001t0011g0362 a0001c0001t0011g0363 |
4 | HG01123.hp2 HG01257.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.452+8350G>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89483586 | |||||||
| chr12:89483663 | T | C | 1 | a0001c0001t0001g0254 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.452+8273A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89483663 | |||||||
| chr12:89483814 | T | G | 1 | a0001c0001t0001g0005 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.452+8122A>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89483814 | |||||||
| chr12:89483861 | T | C | 1 | a0001c0001t0001g0011 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.452+8075A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89483861 | |||||||
| chr12:89483963 | A | G | 1 | a0001c0004t0001g0264 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.452+7973T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89483963 | |||||||
| chr12:89484136 | C | G | 3 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0004g0284 |
3 | HG01167.hp2 HG01891.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.452+7800G>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89484136 | |||||||
| chr12:89484166 | A | G | 75 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0289 others(72): Show |
76 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.452+7770T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89484166 | |||||||
| chr12:89484322 | T | A | 1 | a0001c0001t0001g0148 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.452+7614A>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89484322 | |||||||
| chr12:89484342 | G | C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0236 |
3 | HG02027.hp2 HG02129.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.452+7594C>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89484342 | |||||||
| chr12:89484369 | G | C | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
283 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.452+7567C>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89484369 | |||||||
| chr12:89484933 | A | AGAT | 5 | a0001c0001t0001g0292 a0001c0001t0001g0323 a0001c0001t0001g0324 others(2): Show |
5 | HG02132.hp1 NA18951.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.452+7000_452+7002d others(5): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89484933 | |||||||
| chr12:89485059 | A | T | 1 | a0001c0001t0001g0071 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.452+6877T>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89485059 | |||||||
| chr12:89485187 | T | C | 1 | a0001c0001t0001g0255 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.452+6749A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89485187 | |||||||
| chr12:89485521 | A | G | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
283 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.452+6415T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89485521 | |||||||
| chr12:89485554 | A | T | 279 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(276): Show |
285 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(282): Show |
intron_variant | MODIFIER | c.452+6382T>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89485554 | |||||||
| chr12:89485555 | A | T | 1 | a0001c0001t0001g0010 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.452+6381T>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89485555 | |||||||
| chr12:89485597 | C | T | 1 | a0001c0001t0002g0125 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.452+6339G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89485597 | |||||||
| chr12:89485737 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.452+6199T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89485737 | |||||||
| chr12:89486145 | G | A | 1 | a0001c0001t0001g0333 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.452+5791C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89486145 | |||||||
| chr12:89486237 | G | T | 1 | a0001c0001t0001g0300 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.452+5699C>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89486237 | |||||||
| chr12:89486352 | G | A | 10 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0192 others(7): Show |
10 | HG00099.hp1 HG00639.hp2 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.452+5584C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89486352 | |||||||
| chr12:89486479 | G | C | 3 | a0001c0001t0001g0054 a0001c0001t0001g0061 a0001c0001t0001g0099 |
3 | NA18962.hp2 NA18970.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.452+5457C>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89486479 | |||||||
| chr12:89486866 | A | G | 5 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0001g0312 others(2): Show |
5 | HG02293.hp2 NA18953.hp1 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.452+5070T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89486866 | |||||||
| chr12:89486882 | CTCTT | C | 5 | a0001c0002t0001g0244 a0001c0002t0001g0262 a0001c0002t0001g0263 others(2): Show |
5 | HG00558.hp2 HG00621.hp2 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.452+5050_452+5053d others(6): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89486882 | |||||||
| chr12:89486916 | G | GAC | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.452+5018_452+5019d others(4): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89486916 | |||||||
| chr12:89486956 | A | T | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.452+4980T>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89486956 | |||||||
| chr12:89487042 | C | G | 3 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0004g0284 |
3 | HG01167.hp2 HG01891.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.452+4894G>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89487042 | |||||||
| chr12:89487195 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.452+4741C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89487195 | |||||||
| chr12:89487420 | G | A | 4 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0055 others(1): Show |
5 | HG02258.hp1 HG02970.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.452+4516C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89487420 | |||||||
| chr12:89487457 | A | G | 1 | a0001c0001t0002g0125 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.452+4479T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89487457 | |||||||
| chr12:89487514 | T | C | 2 | a0001c0001t0009g0008 a0001c0001t0009g0009 |
2 | HG02647.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.452+4422A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89487514 | |||||||
| chr12:89487607 | G | T | 1 | a0001c0001t0001g0257 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.452+4329C>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89487607 | |||||||
| chr12:89487634 | T | G | 1 | a0001c0001t0001g0071 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.452+4302A>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89487634 | |||||||
| chr12:89487764 | G | A | 1 | a0001c0001t0001g0300 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.452+4172C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89487764 | |||||||
| chr12:89487782 | A | G | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
283 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.452+4154T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89487782 | |||||||
| chr12:89487787 | C | G | 75 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0289 others(72): Show |
76 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.452+4149G>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89487787 | |||||||
| chr12:89487827 | C | T | 1 | a0001c0001t0008g0360 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.452+4109G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89487827 | |||||||
| chr12:89487946 | C | CT | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(277): Show |
286 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(283): Show |
intron_variant | MODIFIER | c.452+3989_452+3990i others(3): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89487946 | |||||||
| chr12:89487972 | G | A | 1 | a0001c0001t0001g0301 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.452+3964C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89487972 | |||||||
| chr12:89488002 | T | A | 1 | a0001c0001t0001g0010 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.452+3934A>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89488002 | |||||||
| chr12:89488112 | C | T | 1 | a0001c0001t0001g0011 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.452+3824G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89488112 | |||||||
| chr12:89488158 | TACA | T | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(170): Show |
177 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.452+3775_452+3777d others(5): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89488158 | |||||||
| chr12:89488169 | C | T | 3 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0004g0284 |
3 | HG01167.hp2 HG01891.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.452+3767G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89488169 | |||||||
| chr12:89488263 | C | A | 4 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(1): Show |
4 | HG01109.hp1 HG02630.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.452+3673G>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89488263 | |||||||
| chr12:89488675 | C | T | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.452+3261G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89488675 | |||||||
| chr12:89488763 | G | A | 4 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(1): Show |
4 | HG01109.hp1 HG02630.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.452+3173C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89488763 | |||||||
| chr12:89488768 | T | C | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(277): Show |
286 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(283): Show |
intron_variant | MODIFIER | c.452+3168A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89488768 | |||||||
| chr12:89488792 | C | T | 3 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0004g0284 |
3 | HG01167.hp2 HG01891.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.452+3144G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89488792 | |||||||
| chr12:89489333 | C | T | 3 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0201 |
3 | HG01167.hp1 HG01169.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.452+2603G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89489333 | |||||||
| chr12:89489496 | TA | T | 3 | a0001c0001t0005g0043 a0001c0001t0005g0044 a0001c0001t0005g0045 |
3 | HG02615.hp1 HG03540.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.452+2439delT | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89489496 | |||||||
| chr12:89489509 | T | A | 1 | a0001c0001t0001g0071 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.452+2427A>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89489509 | |||||||
| chr12:89489525 | A | G | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(62): Show |
68 | HG00423.hp2 HG00673.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.452+2411T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89489525 | |||||||
| chr12:89489697 | C | A | 1 | a0001c0001t0001g0034 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.452+2239G>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89489697 | |||||||
| chr12:89489742 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.452+2194G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89489742 | |||||||
| chr12:89489813 | A | G | 1 | a0001c0001t0002g0156 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.452+2123T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89489813 | |||||||
| chr12:89489818 | A | G | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
283 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.452+2118T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89489818 | |||||||
| chr12:89489991 | C | G | 1 | a0001c0001t0001g0306 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.452+1945G>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89489991 | |||||||
| chr12:89490053 | G | T | 3 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0004g0284 |
3 | HG01167.hp2 HG01891.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.452+1883C>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89490053 | |||||||
| chr12:89490287 | T | C | 1 | a0001c0001t0001g0221 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.452+1649A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89490287 | |||||||
| chr12:89490501 | C | T | 75 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0289 others(72): Show |
76 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.452+1435G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89490501 | |||||||
| chr12:89490517 | G | A | 75 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0289 others(72): Show |
76 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.452+1419C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89490517 | |||||||
| chr12:89490616 | A | T | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.452+1320T>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89490616 | |||||||
| chr12:89490817 | G | A | 1 | a0001c0001t0002g0133 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.452+1119C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89490817 | |||||||
| chr12:89490910 | ATCCAAGC others(15): Show |
A | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(199): Show |
207 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(204): Show |
intron_variant | MODIFIER | c.452+1004_452+1025d others(24): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89490910 | |||||||
| chr12:89491052 | T | A | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(62): Show |
68 | HG00423.hp2 HG00673.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.452+884A>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89491052 | |||||||
| chr12:89491460 | C | T | 3 | a0001c0001t0006g0226 a0001c0001t0006g0227 a0001c0001t0006g0228 |
3 | HG01070.hp2 HG01361.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.452+476G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89491460 | |||||||
| chr12:89491489 | G | T | 15 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0192 others(12): Show |
15 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.452+447C>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89491489 | |||||||
| chr12:89491626 | AAAAAAAA others(6): Show |
A | 1 | a0001c0001t0002g0150 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.452+297_452+309del others(13): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89491626 | |||||||
| chr12:89491665 | C | T | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(62): Show |
68 | HG00423.hp2 HG00673.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.452+271G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89491665 | |||||||
| chr12:89491694 | C | T | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(193): Show |
201 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.452+242G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89491694 | |||||||
| chr12:89491696 | T | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(185): Show |
193 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(190): Show |
intron_variant | MODIFIER | c.452+240A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89491696 | |||||||
| chr12:89491798 | C | T | 3 | a0001c0001t0006g0226 a0001c0001t0006g0227 a0001c0001t0006g0228 |
3 | HG01070.hp2 HG01361.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.452+138G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89491798 | |||||||
| chr12:89491871 | G | T | 62 | a0001c0001t0001g0103 a0001c0001t0001g0111 a0001c0001t0001g0116 others(59): Show |
62 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.452+65C>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 4/11 | chr12 | 89491871 | |||||||
| chr12:89492146 | C | A | 75 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0289 others(72): Show |
76 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.273-31G>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 3/11 | chr12 | 89492146 | |||||||
| chr12:89492165 | T | C | 77 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0120 others(74): Show |
78 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.273-50A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 3/11 | chr12 | 89492165 | |||||||
| chr12:89492278 | C | G | 1 | a0001c0001t0002g0058 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.273-163G>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 3/11 | chr12 | 89492278 | |||||||
| chr12:89492507 | T | C | 1 | a0001c0001t0001g0242 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.273-392A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 3/11 | chr12 | 89492507 | |||||||
| chr12:89492548 | C | G | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
195 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.273-433G>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 3/11 | chr12 | 89492548 | |||||||
| chr12:89492717 | C | T | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(62): Show |
68 | HG00423.hp2 HG00673.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.273-602G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 3/11 | chr12 | 89492717 | |||||||
| chr12:89492801 | T | A | 75 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0289 others(72): Show |
76 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.273-686A>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 3/11 | chr12 | 89492801 | |||||||
| chr12:89492862 | G | A | 2 | a0001c0001t0001g0053 a0001c0001t0001g0064 |
2 | HG00741.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.273-747C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 3/11 | chr12 | 89492862 | |||||||
| chr12:89492960 | T | C | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.273-845A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 3/11 | chr12 | 89492960 | |||||||
| chr12:89492984 | C | T | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(194): Show |
202 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.273-869G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 3/11 | chr12 | 89492984 | |||||||
| chr12:89493420 | G | A | 3 | a0001c0001t0002g0124 a0001c0001t0002g0157 a0001c0001t0002g0158 |
3 | NA18612.hp2 NA18960.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.273-1305C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 3/11 | chr12 | 89493420 | |||||||
| chr12:89493439 | C | T | 1 | a0001c0001t0001g0185 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.273-1324G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 3/11 | chr12 | 89493439 | |||||||
| chr12:89493595 | A | G | 2 | a0001c0001t0001g0053 a0001c0001t0001g0064 |
2 | HG00741.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.273-1480T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 3/11 | chr12 | 89493595 | |||||||
| chr12:89493681 | C | T | 6 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(3): Show |
6 | HG00673.hp1 HG02165.hp1 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.273-1566G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 3/11 | chr12 | 89493681 | |||||||
| chr12:89493730 | T | A | 2 | a0001c0001t0001g0215 a0001c0001t0001g0218 |
2 | HG00673.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.273-1615A>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 3/11 | chr12 | 89493730 | |||||||
| chr12:89493872 | T | C | 75 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0289 others(72): Show |
76 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.273-1757A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 3/11 | chr12 | 89493872 | |||||||
| chr12:89494207 | T | TTTTA | 19 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0191 others(16): Show |
19 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.273-2096_273-2093d others(6): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 3/11 | chr12 | 89494207 | |||||||
| chr12:89494663 | G | C | 1 | a0002c0003t0001g0288 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.272+2508C>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 3/11 | chr12 | 89494663 | |||||||
| chr12:89494812 | C | T | 62 | a0001c0001t0001g0103 a0001c0001t0001g0111 a0001c0001t0001g0116 others(59): Show |
62 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.272+2359G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 3/11 | chr12 | 89494812 | |||||||
| chr12:89494873 | T | C | 6 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0003g0042 others(3): Show |
6 | HG02572.hp1 HG02615.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.272+2298A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 3/11 | chr12 | 89494873 | |||||||
| chr12:89494915 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.272+2256A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 3/11 | chr12 | 89494915 | |||||||
| chr12:89494945 | A | G | 1 | a0001c0001t0001g0082 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.272+2226T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 3/11 | chr12 | 89494945 | |||||||
| chr12:89494995 | G | C | 1 | a0001c0001t0001g0224 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.272+2176C>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 3/11 | chr12 | 89494995 | |||||||
| chr12:89495013 | T | C | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(270): Show |
279 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(276): Show |
intron_variant | MODIFIER | c.272+2158A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 3/11 | chr12 | 89495013 | |||||||
| chr12:89495059 | G | A | 1 | a0001c0002t0001g0244 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.272+2112C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 3/11 | chr12 | 89495059 | |||||||
| chr12:89495195 | C | T | 4 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(1): Show |
4 | HG01109.hp1 HG02630.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.272+1976G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 3/11 | chr12 | 89495195 | |||||||
| chr12:89495350 | A | C | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(277): Show |
286 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(283): Show |
intron_variant | MODIFIER | c.272+1821T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 3/11 | chr12 | 89495350 | |||||||
| chr12:89495643 | G | C | 3 | a0001c0001t0001g0059 a0001c0001t0001g0062 a0001c0001t0001g0100 |
3 | HG03017.hp1 HG04115.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.272+1528C>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 3/11 | chr12 | 89495643 | |||||||
| chr12:89495674 | T | C | 1 | a0001c0001t0001g0077 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.272+1497A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 3/11 | chr12 | 89495674 | |||||||
| chr12:89495755 | G | GTAT | 3 | a0001c0001t0001g0151 a0001c0001t0001g0237 a0001c0001t0002g0135 |
3 | HG03704.hp1 NA18963.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.272+1413_272+1415d others(5): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 3/11 | chr12 | 89495755 | |||||||
| chr12:89495869 | C | T | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.272+1302G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 3/11 | chr12 | 89495869 | |||||||
| chr12:89495919 | G | A | 1 | a0001c0001t0001g0275 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.272+1252C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 3/11 | chr12 | 89495919 | |||||||
| chr12:89495975 | G | C | 1 | a0001c0001t0002g0021 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.272+1196C>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 3/11 | chr12 | 89495975 | |||||||
| chr12:89496178 | G | A | 5 | a0001c0001t0001g0004 a0001c0001t0001g0104 a0001c0001t0001g0105 others(2): Show |
6 | HG02486.hp1 HG02723.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.272+993C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 3/11 | chr12 | 89496178 | |||||||
| chr12:89496384 | T | C | 1 | a0001c0001t0001g0321 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.272+787A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 3/11 | chr12 | 89496384 | |||||||
| chr12:89496487 | C | T | 7 | a0001c0001t0001g0337 a0001c0001t0001g0338 a0001c0001t0001g0339 others(4): Show |
7 | HG00323.hp2 HG00738.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.272+684G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 3/11 | chr12 | 89496487 | |||||||
| chr12:89496720 | A | G | 1 | a0001c0001t0001g0309 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.272+451T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 3/11 | chr12 | 89496720 | |||||||
| chr12:89496813 | G | A | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
283 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.272+358C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 3/11 | chr12 | 89496813 | |||||||
| chr12:89497007 | G | GA | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(62): Show |
68 | HG00423.hp2 HG00673.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.272+163dupT | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 3/11 | chr12 | 89497007 | |||||||
| chr12:89497391 | T | C | 1 | a0001c0001t0001g0306 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.101-49A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89497391 | |||||||
| chr12:89497450 | C | A | 5 | a0001c0001t0001g0292 a0001c0001t0001g0323 a0001c0001t0001g0324 others(2): Show |
5 | HG02132.hp1 NA18951.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.101-108G>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89497450 | |||||||
| chr12:89497539 | T | C | 1 | a0001c0001t0001g0268 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.101-197A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89497539 | |||||||
| chr12:89497589 | G | A | 75 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0289 others(72): Show |
76 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.101-247C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89497589 | |||||||
| chr12:89497697 | T | G | 75 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0289 others(72): Show |
76 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.101-355A>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89497697 | |||||||
| chr12:89497895 | G | A | 1 | a0001c0004t0001g0264 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.101-553C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89497895 | |||||||
| chr12:89498146 | T | C | 1 | a0001c0001t0001g0063 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.101-804A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89498146 | |||||||
| chr12:89498152 | T | A | 4 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(1): Show |
4 | HG01109.hp1 HG02630.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-810A>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89498152 | |||||||
| chr12:89498238 | G | A | 1 | a0001c0001t0004g0287 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.101-896C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89498238 | |||||||
| chr12:89498242 | G | C | 5 | a0001c0001t0001g0292 a0001c0001t0001g0323 a0001c0001t0001g0324 others(2): Show |
5 | HG02132.hp1 NA18951.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.101-900C>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89498242 | |||||||
| chr12:89498374 | T | C | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(195): Show |
203 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.101-1032A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89498374 | |||||||
| chr12:89498383 | T | C | 3 | a0001c0001t0006g0226 a0001c0001t0006g0227 a0001c0001t0006g0228 |
3 | HG01070.hp2 HG01361.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.101-1041A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89498383 | |||||||
| chr12:89498481 | C | T | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
283 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.101-1139G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89498481 | |||||||
| chr12:89498584 | C | T | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-1242G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89498584 | |||||||
| chr12:89498601 | T | A | 1 | a0001c0001t0001g0011 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.101-1259A>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89498601 | |||||||
| chr12:89498824 | G | A | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-1482C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89498824 | |||||||
| chr12:89498955 | T | G | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-1613A>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89498955 | |||||||
| chr12:89499006 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.101-1664A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89499006 | |||||||
| chr12:89499012 | G | A | 1 | a0002c0003t0001g0288 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.101-1670C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89499012 | |||||||
| chr12:89499014 | G | A | 1 | a0001c0001t0002g0165 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.101-1672C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89499014 | |||||||
| chr12:89499213 | T | C | 1 | a0001c0001t0001g0212 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.101-1871A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89499213 | |||||||
| chr12:89499309 | T | G | 63 | a0001c0001t0001g0103 a0001c0001t0001g0111 a0001c0001t0001g0116 others(60): Show |
63 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.101-1967A>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89499309 | |||||||
| chr12:89499368 | G | A | 67 | a0001c0001t0001g0103 a0001c0001t0001g0111 a0001c0001t0001g0116 others(64): Show |
67 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.101-2026C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89499368 | |||||||
| chr12:89499420 | A | C | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(195): Show |
203 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.101-2078T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89499420 | |||||||
| chr12:89499520 | GA | G | 75 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0289 others(72): Show |
76 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.101-2179delT | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89499520 | |||||||
| chr12:89499571 | T | C | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
195 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.101-2229A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89499571 | |||||||
| chr12:89499619 | AT | A | 75 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0289 others(72): Show |
76 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.101-2278delA | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89499619 | |||||||
| chr12:89499621 | T | G | 3 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 |
3 | HG01192.hp1 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.101-2279A>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89499621 | |||||||
| chr12:89499678 | A | G | 2 | a0001c0001t0001g0291 a0001c0001t0001g0308 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.101-2336T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89499678 | |||||||
| chr12:89499925 | C | A | 3 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0004g0284 |
3 | HG01167.hp2 HG01891.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.101-2583G>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89499925 | |||||||
| chr12:89499934 | C | T | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-2592G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89499934 | |||||||
| chr12:89499935 | A | G | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(277): Show |
286 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(283): Show |
intron_variant | MODIFIER | c.101-2593T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89499935 | |||||||
| chr12:89499943 | G | A | 1 | a0001c0001t0001g0326 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.101-2601C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89499943 | |||||||
| chr12:89500012 | A | C | 5 | a0001c0002t0001g0244 a0001c0002t0001g0262 a0001c0002t0001g0263 others(2): Show |
5 | HG00558.hp2 HG00621.hp2 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.101-2670T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89500012 | |||||||
| chr12:89500100 | T | C | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(277): Show |
286 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(283): Show |
intron_variant | MODIFIER | c.101-2758A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89500100 | |||||||
| chr12:89500148 | A | G | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(277): Show |
286 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(283): Show |
intron_variant | MODIFIER | c.101-2806T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89500148 | |||||||
| chr12:89500326 | C | A | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
195 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.101-2984G>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89500326 | |||||||
| chr12:89500361 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.101-3019G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89500361 | |||||||
| chr12:89500490 | T | C | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
283 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.101-3148A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89500490 | |||||||
| chr12:89500550 | A | C | 1 | a0001c0001t0001g0122 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.101-3208T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89500550 | |||||||
| chr12:89501349 | A | C | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-4007T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89501349 | |||||||
| chr12:89501598 | C | A | 1 | a0001c0001t0001g0041 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.101-4256G>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89501598 | |||||||
| chr12:89501684 | G | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(162): Show |
169 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.101-4342C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89501684 | |||||||
| chr12:89501728 | G | A | 8 | a0001c0001t0001g0032 a0001c0001t0001g0266 a0001c0001t0001g0268 others(5): Show |
8 | HG00408.hp2 HG01943.hp2 HG01993.hp1 others(5): Show |
intron_variant | MODIFIER | c.101-4386C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89501728 | |||||||
| chr12:89501838 | A | C | 1 | a0001c0001t0001g0348 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.101-4496T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89501838 | |||||||
| chr12:89501917 | G | A | 1 | a0001c0001t0003g0042 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.101-4575C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89501917 | |||||||
| chr12:89501942 | C | G | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(277): Show |
286 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(283): Show |
intron_variant | MODIFIER | c.101-4600G>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89501942 | |||||||
| chr12:89502206 | T | G | 1 | a0001c0001t0001g0103 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.101-4864A>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89502206 | |||||||
| chr12:89502322 | G | A | 1 | a0001c0001t0001g0230 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.101-4980C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89502322 | |||||||
| chr12:89502623 | T | TGGATCTT others(10): Show |
4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-5298_101-5282d others(19): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89502623 | |||||||
| chr12:89502836 | T | A | 3 | a0001c0001t0006g0226 a0001c0001t0006g0227 a0001c0001t0006g0228 |
3 | HG01070.hp2 HG01361.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.101-5494A>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89502836 | |||||||
| chr12:89502848 | G | T | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-5506C>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89502848 | |||||||
| chr12:89502860 | A | G | 1 | a0001c0001t0001g0209 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.101-5518T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89502860 | |||||||
| chr12:89503016 | C | A | 4 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(1): Show |
4 | HG01109.hp1 HG02630.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-5674G>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89503016 | |||||||
| chr12:89503078 | T | TCTATCC | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(112): Show |
119 | HG00099.hp1 HG00423.hp2 HG00639.hp2 others(116): Show |
intron_variant | MODIFIER | c.101-5742_101-5737d others(8): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89503078 | |||||||
| chr12:89503078 | T | TCTATCCC others(5): Show |
154 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0022 others(151): Show |
156 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.101-5748_101-5737d others(14): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89503078 | |||||||
| chr12:89503078 | T | TCTATCCC others(11): Show |
2 | a0001c0001t0001g0110 a0001c0001t0001g0302 |
2 | HG02615.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.101-5754_101-5737d others(20): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89503078 | |||||||
| chr12:89503109 | CTCTCTCC others(6): Show |
C | 1 | a0001c0001t0001g0285 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.101-5780_101-5768d others(15): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89503109 | |||||||
| chr12:89503120 | C | T | 75 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0289 others(72): Show |
76 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.101-5778G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89503120 | |||||||
| chr12:89503124 | C | A | 1 | a0001c0001t0001g0285 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.101-5782G>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89503124 | |||||||
| chr12:89503130 | C | A | 1 | a0001c0001t0001g0285 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.101-5788G>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89503130 | |||||||
| chr12:89503140 | T | C | 1 | a0001c0001t0001g0285 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.101-5798A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89503140 | |||||||
| chr12:89503141 | T | C | 1 | a0001c0001t0001g0285 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.101-5799A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89503141 | |||||||
| chr12:89503146 | A | G | 1 | a0001c0001t0001g0285 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.101-5804T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89503146 | |||||||
| chr12:89503224 | C | G | 1 | a0001c0001t0004g0040 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.101-5882G>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89503224 | |||||||
| chr12:89503226 | T | C | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(270): Show |
279 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(276): Show |
intron_variant | MODIFIER | c.101-5884A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89503226 | |||||||
| chr12:89503251 | A | C | 63 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(60): Show |
66 | HG00423.hp2 HG00673.hp2 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.101-5909T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89503251 | |||||||
| chr12:89503263 | C | T | 92 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0023 others(89): Show |
93 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.101-5921G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89503263 | |||||||
| chr12:89503354 | T | G | 1 | a0001c0001t0001g0243 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.101-6012A>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89503354 | |||||||
| chr12:89503384 | C | G | 75 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0289 others(72): Show |
76 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.101-6042G>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89503384 | |||||||
| chr12:89503508 | C | T | 2 | a0001c0001t0008g0359 a0001c0001t0008g0361 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.101-6166G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89503508 | |||||||
| chr12:89503509 | A | G | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(268): Show |
277 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(274): Show |
intron_variant | MODIFIER | c.101-6167T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89503509 | |||||||
| chr12:89503527 | T | C | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
283 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.101-6185A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89503527 | |||||||
| chr12:89503557 | C | T | 75 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0289 others(72): Show |
76 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.101-6215G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89503557 | |||||||
| chr12:89503562 | C | T | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-6220G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89503562 | |||||||
| chr12:89503611 | C | T | 75 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0289 others(72): Show |
76 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.101-6269G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89503611 | |||||||
| chr12:89503694 | C | T | 3 | a0001c0001t0006g0226 a0001c0001t0006g0227 a0001c0001t0006g0228 |
3 | HG01070.hp2 HG01361.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.101-6352G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89503694 | |||||||
| chr12:89503695 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.101-6353G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89503695 | |||||||
| chr12:89503723 | C | T | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(270): Show |
279 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(276): Show |
intron_variant | MODIFIER | c.101-6381G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89503723 | |||||||
| chr12:89503733 | G | GTCTGAGA others(33): Show |
1 | a0001c0001t0001g0268 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.101-6431_101-6392d others(42): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89503733 | |||||||
| chr12:89503733 | GTCTGAGA others(33): Show |
G | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
283 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.101-6431_101-6392d others(42): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89503733 | |||||||
| chr12:89503797 | G | A | 3 | a0001c0001t0006g0226 a0001c0001t0006g0227 a0001c0001t0006g0228 |
3 | HG01070.hp2 HG01361.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.101-6455C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89503797 | |||||||
| chr12:89503809 | C | T | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-6467G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89503809 | |||||||
| chr12:89503813 | A | G | 6 | a0001c0001t0001g0079 a0001c0001t0001g0209 a0001c0001t0001g0210 others(3): Show |
6 | HG01070.hp2 HG01361.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.101-6471T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89503813 | |||||||
| chr12:89503877 | G | A | 1 | a0001c0001t0001g0256 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.101-6535C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89503877 | |||||||
| chr12:89503892 | T | C | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(277): Show |
286 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(283): Show |
intron_variant | MODIFIER | c.101-6550A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89503892 | |||||||
| chr12:89503922 | G | T | 1 | a0001c0001t0001g0010 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.101-6580C>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89503922 | |||||||
| chr12:89503924 | A | C | 1 | a0001c0001t0001g0010 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.101-6582T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89503924 | |||||||
| chr12:89503928 | A | G | 1 | a0001c0001t0001g0283 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.101-6586T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89503928 | |||||||
| chr12:89503929 | C | G | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(195): Show |
203 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.101-6587G>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89503929 | |||||||
| chr12:89503949 | G | A | 2 | a0001c0001t0001g0337 a0001c0001t0001g0341 |
2 | HG01081.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.101-6607C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89503949 | |||||||
| chr12:89503956 | C | T | 4 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0055 others(1): Show |
5 | HG02258.hp1 HG02970.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.101-6614G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89503956 | |||||||
| chr12:89503961 | G | C | 1 | a0001c0001t0002g0112 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.101-6619C>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89503961 | |||||||
| chr12:89503973 | G | A | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(270): Show |
279 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(276): Show |
intron_variant | MODIFIER | c.101-6631C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89503973 | |||||||
| chr12:89504083 | G | T | 2 | a0001c0001t0001g0306 a0001c0001t0001g0344 |
2 | HG03017.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.101-6741C>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89504083 | |||||||
| chr12:89504127 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.101-6785G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89504127 | |||||||
| chr12:89504271 | T | C | 1 | a0001c0001t0001g0110 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.101-6929A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89504271 | |||||||
| chr12:89504285 | C | T | 1 | a0001c0001t0001g0337 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.101-6943G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89504285 | |||||||
| chr12:89504366 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.101-7024G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89504366 | |||||||
| chr12:89504370 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.101-7028C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89504370 | |||||||
| chr12:89504563 | C | T | 3 | a0001c0001t0001g0233 a0001c0001t0010g0234 a0001c0001t0010g0235 |
3 | HG02258.hp2 HG02922.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.101-7221G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89504563 | |||||||
| chr12:89504600 | A | AT | 267 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(264): Show |
273 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(270): Show |
intron_variant | MODIFIER | c.101-7259dupA | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89504600 | |||||||
| chr12:89504601 | T | TTA | 3 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 |
3 | HG01192.hp1 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.101-7260_101-7259i others(4): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89504601 | |||||||
| chr12:89504602 | A | T | 3 | a0001c0001t0001g0201 a0001c0001t0002g0113 a0001c0001t0002g0158 |
3 | HG01169.hp1 NA18612.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.101-7260T>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89504602 | |||||||
| chr12:89504633 | C | T | 1 | a0001c0001t0001g0081 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.101-7291G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89504633 | |||||||
| chr12:89504989 | G | C | 1 | a0001c0001t0002g0150 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.101-7647C>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89504989 | |||||||
| chr12:89505028 | C | T | 3 | a0001c0001t0001g0054 a0001c0001t0001g0061 a0001c0001t0001g0099 |
3 | NA18962.hp2 NA18970.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.101-7686G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89505028 | |||||||
| chr12:89505083 | A | T | 1 | a0001c0001t0001g0231 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.101-7741T>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89505083 | |||||||
| chr12:89505168 | T | G | 1 | a0001c0001t0002g0232 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.101-7826A>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89505168 | |||||||
| chr12:89505326 | A | C | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
195 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.101-7984T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89505326 | |||||||
| chr12:89505381 | G | A | 6 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0003g0042 others(3): Show |
6 | HG02572.hp1 HG02615.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.101-8039C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89505381 | |||||||
| chr12:89505492 | T | C | 1 | a0001c0001t0004g0284 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.101-8150A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89505492 | |||||||
| chr12:89505503 | A | C | 1 | a0001c0001t0001g0050 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.101-8161T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89505503 | |||||||
| chr12:89505631 | C | G | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-8289G>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89505631 | |||||||
| chr12:89505719 | A | G | 3 | a0001c0001t0001g0079 a0001c0001t0009g0008 a0001c0001t0009g0009 |
3 | HG02622.hp1 HG02647.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.101-8377T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89505719 | |||||||
| chr12:89505850 | G | C | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(270): Show |
279 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(276): Show |
intron_variant | MODIFIER | c.101-8508C>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89505850 | |||||||
| chr12:89505925 | A | G | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
283 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.101-8583T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89505925 | |||||||
| chr12:89506075 | T | A | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
283 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.101-8733A>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89506075 | |||||||
| chr12:89506135 | G | C | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
283 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.101-8793C>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89506135 | |||||||
| chr12:89506142 | G | A | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-8800C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89506142 | |||||||
| chr12:89506159 | G | C | 4 | a0001c0001t0001g0191 a0001c0001t0001g0206 a0001c0001t0001g0207 others(1): Show |
4 | HG02280.hp2 HG02970.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-8817C>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89506159 | |||||||
| chr12:89506297 | T | C | 1 | a0001c0001t0002g0164 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.101-8955A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89506297 | |||||||
| chr12:89506363 | A | G | 92 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0023 others(89): Show |
93 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.101-9021T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89506363 | |||||||
| chr12:89506622 | G | GCCCCCCC others(18): Show |
1 | a0001c0001t0001g0094 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.101-9281_101-9280i others(27): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89506622 | |||||||
| chr12:89506708 | A | G | 1 | a0001c0002t0001g0244 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.101-9366T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89506708 | |||||||
| chr12:89506863 | A | G | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(270): Show |
279 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(276): Show |
intron_variant | MODIFIER | c.101-9521T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89506863 | |||||||
| chr12:89507057 | G | A | 3 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0004g0284 |
3 | HG01167.hp2 HG01891.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.101-9715C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89507057 | |||||||
| chr12:89507077 | C | A | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | NA18964.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.101-9735G>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89507077 | |||||||
| chr12:89507091 | G | A | 1 | a0001c0001t0001g0327 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.101-9749C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89507091 | |||||||
| chr12:89507093 | A | C | 1 | a0001c0001t0001g0347 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.101-9751T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89507093 | |||||||
| chr12:89507169 | G | C | 5 | a0001c0001t0002g0124 a0001c0001t0002g0156 a0001c0001t0002g0157 others(2): Show |
5 | HG01081.hp2 HG01928.hp1 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.101-9827C>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89507169 | |||||||
| chr12:89507194 | G | T | 1 | a0001c0001t0002g0232 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.101-9852C>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89507194 | |||||||
| chr12:89507266 | C | CA | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(153): Show |
159 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.101-9925dupT | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89507266 | |||||||
| chr12:89507266 | C | CAA | 62 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0012 others(59): Show |
63 | HG00423.hp1 HG00423.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.101-9926_101-9925d others(4): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89507266 | |||||||
| chr12:89507266 | CA | C | 68 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0268 others(65): Show |
69 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.101-9925delT | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89507266 | |||||||
| chr12:89507468 | A | T | 1 | a0001c0001t0001g0080 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.101-10126T>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89507468 | |||||||
| chr12:89507702 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.101-10360C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89507702 | |||||||
| chr12:89507760 | A | G | 1 | a0001c0001t0001g0053 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.101-10418T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89507760 | |||||||
| chr12:89507840 | G | A | 63 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(60): Show |
66 | HG00423.hp2 HG00673.hp2 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.101-10498C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89507840 | |||||||
| chr12:89507965 | A | G | 1 | a0001c0001t0001g0336 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.101-10623T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89507965 | |||||||
| chr12:89508045 | T | A | 2 | a0001c0001t0002g0154 a0001c0001t0002g0155 |
2 | NA19056.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.101-10703A>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89508045 | |||||||
| chr12:89508107 | T | C | 1 | a0001c0001t0004g0040 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.101-10765A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89508107 | |||||||
| chr12:89508123 | G | A | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-10781C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89508123 | |||||||
| chr12:89508442 | T | C | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
195 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.101-11100A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89508442 | |||||||
| chr12:89508491 | G | A | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-11149C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89508491 | |||||||
| chr12:89508499 | T | G | 1 | a0001c0001t0001g0050 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.101-11157A>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89508499 | |||||||
| chr12:89508558 | G | A | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(195): Show |
203 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.101-11216C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89508558 | |||||||
| chr12:89508626 | A | G | 1 | a0001c0001t0001g0215 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.101-11284T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89508626 | |||||||
| chr12:89508827 | G | A | 75 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0289 others(72): Show |
76 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.101-11485C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89508827 | |||||||
| chr12:89509017 | C | T | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(270): Show |
279 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(276): Show |
intron_variant | MODIFIER | c.101-11675G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89509017 | |||||||
| chr12:89509093 | C | A | 4 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0055 others(1): Show |
5 | HG02258.hp1 HG02970.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.101-11751G>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89509093 | |||||||
| chr12:89509131 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.101-11789A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89509131 | |||||||
| chr12:89509224 | T | C | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-11882A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89509224 | |||||||
| chr12:89509428 | C | G | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(195): Show |
203 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.101-12086G>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89509428 | |||||||
| chr12:89509438 | T | C | 12 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0192 others(9): Show |
12 | HG00099.hp1 HG00639.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.101-12096A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89509438 | |||||||
| chr12:89509651 | C | A | 2 | a0001c0001t0001g0010 a0001c0001t0004g0040 |
2 | HG00639.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.101-12309G>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89509651 | |||||||
| chr12:89509653 | T | C | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-12311A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89509653 | |||||||
| chr12:89509720 | T | A | 3 | a0001c0001t0006g0226 a0001c0001t0006g0227 a0001c0001t0006g0228 |
3 | HG01070.hp2 HG01361.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.101-12378A>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89509720 | |||||||
| chr12:89509738 | G | A | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-12396C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89509738 | |||||||
| chr12:89509813 | T | G | 1 | a0001c0001t0002g0158 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.101-12471A>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89509813 | |||||||
| chr12:89509825 | C | T | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-12483G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89509825 | |||||||
| chr12:89509834 | T | C | 4 | a0001c0002t0001g0262 a0001c0002t0001g0263 a0001c0002t0001g0267 others(1): Show |
4 | HG00558.hp2 HG00621.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-12492A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89509834 | |||||||
| chr12:89509839 | T | C | 1 | a0001c0001t0015g0358 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.101-12497A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89509839 | |||||||
| chr12:89509855 | G | GT | 4 | a0001c0001t0001g0057 a0001c0001t0001g0197 a0001c0001t0002g0124 others(1): Show |
4 | HG01261.hp2 HG02258.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-12514_101-1251 others(5): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89509855 | |||||||
| chr12:89509856 | G | GT | 5 | a0001c0001t0001g0030 a0001c0001t0001g0050 a0001c0001t0001g0214 others(2): Show |
5 | HG01175.hp2 HG04184.hp1 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.101-12515dupA | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89509856 | |||||||
| chr12:89509856 | G | T | 191 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(188): Show |
196 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.101-12514C>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89509856 | |||||||
| chr12:89509875 | T | G | 1 | a0001c0001t0001g0095 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.101-12533A>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89509875 | |||||||
| chr12:89509877 | A | C | 113 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0022 others(110): Show |
114 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.101-12535T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89509877 | |||||||
| chr12:89509920 | A | C | 1 | a0001c0001t0001g0192 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.101-12578T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89509920 | |||||||
| chr12:89510012 | A | AT | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(268): Show |
277 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(274): Show |
intron_variant | MODIFIER | c.101-12671dupA | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89510012 | |||||||
| chr12:89510183 | A | T | 4 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(1): Show |
4 | HG01109.hp1 HG02630.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-12841T>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89510183 | |||||||
| chr12:89510209 | C | T | 2 | a0001c0001t0001g0059 a0001c0001t0001g0100 |
2 | HG03017.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.101-12867G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89510209 | |||||||
| chr12:89510211 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.101-12869G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89510211 | |||||||
| chr12:89510269 | A | G | 1 | a0001c0001t0001g0041 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.101-12927T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89510269 | |||||||
| chr12:89510275 | C | A | 63 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(60): Show |
66 | HG00423.hp2 HG00673.hp2 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.101-12933G>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89510275 | |||||||
| chr12:89510390 | C | T | 63 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(60): Show |
66 | HG00423.hp2 HG00673.hp2 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.101-13048G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89510390 | |||||||
| chr12:89510542 | C | G | 1 | a0001c0001t0001g0332 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.101-13200G>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89510542 | |||||||
| chr12:89510753 | T | C | 14 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0061 others(11): Show |
14 | HG00673.hp2 HG00735.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.101-13411A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89510753 | |||||||
| chr12:89510756 | T | G | 1 | a0001c0001t0001g0005 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.101-13414A>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89510756 | |||||||
| chr12:89510763 | C | CTTTT | 61 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(58): Show |
64 | HG00423.hp2 HG00673.hp2 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.101-13425_101-1342 others(8): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89510763 | |||||||
| chr12:89510763 | C | CTTTTTT | 69 | a0001c0001t0001g0103 a0001c0001t0001g0108 a0001c0001t0001g0111 others(66): Show |
69 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.101-13427_101-1342 others(10): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89510763 | |||||||
| chr12:89510763 | C | CTTTTTTT | 121 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(118): Show |
124 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(121): Show |
intron_variant | MODIFIER | c.101-13428_101-1342 others(11): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89510763 | |||||||
| chr12:89510763 | C | CTTTTTTT others(1): Show |
18 | a0001c0001t0001g0024 a0001c0001t0001g0039 a0001c0001t0001g0297 others(15): Show |
18 | HG00323.hp2 HG00639.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.101-13429_101-1342 others(12): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89510763 | |||||||
| chr12:89510782 | G | C | 1 | a0001c0001t0001g0056 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.101-13440C>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89510782 | |||||||
| chr12:89510819 | A | G | 3 | a0001c0001t0006g0226 a0001c0001t0006g0227 a0001c0001t0006g0228 |
3 | HG01070.hp2 HG01361.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.101-13477T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89510819 | |||||||
| chr12:89510836 | C | T | 1 | a0001c0001t0001g0005 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.101-13494G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89510836 | |||||||
| chr12:89510839 | C | T | 63 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(60): Show |
66 | HG00423.hp2 HG00673.hp2 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.101-13497G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89510839 | |||||||
| chr12:89510921 | T | A | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(270): Show |
279 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(276): Show |
intron_variant | MODIFIER | c.101-13579A>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89510921 | |||||||
| chr12:89510972 | C | G | 1 | a0001c0001t0001g0079 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.101-13630G>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89510972 | |||||||
| chr12:89511007 | G | A | 3 | a0001c0001t0006g0226 a0001c0001t0006g0227 a0001c0001t0006g0228 |
3 | HG01070.hp2 HG01361.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.101-13665C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89511007 | |||||||
| chr12:89511007 | G | C | 5 | a0001c0001t0002g0124 a0001c0001t0002g0156 a0001c0001t0002g0157 others(2): Show |
5 | HG01081.hp2 HG01928.hp1 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.101-13665C>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89511007 | |||||||
| chr12:89511243 | T | C | 1 | a0001c0001t0001g0054 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.100+13877A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89511243 | |||||||
| chr12:89511315 | C | G | 1 | a0001c0001t0003g0351 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.100+13805G>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89511315 | |||||||
| chr12:89511386 | A | C | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+13734T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89511386 | |||||||
| chr12:89511415 | C | CA | 15 | a0001c0001t0001g0004 a0001c0001t0001g0047 a0001c0001t0001g0048 others(12): Show |
16 | HG01167.hp2 HG01192.hp1 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.100+13704dupT | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89511415 | |||||||
| chr12:89511415 | CA | C | 12 | a0001c0001t0001g0014 a0001c0001t0001g0061 a0001c0001t0001g0192 others(9): Show |
12 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.100+13704delT | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89511415 | |||||||
| chr12:89511611 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.100+13509C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89511611 | |||||||
| chr12:89511760 | C | T | 278 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(275): Show |
284 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(281): Show |
intron_variant | MODIFIER | c.100+13360G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89511760 | |||||||
| chr12:89511828 | T | C | 1 | a0001c0004t0001g0264 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.100+13292A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89511828 | |||||||
| chr12:89511879 | C | A | 3 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 |
3 | HG01192.hp1 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.100+13241G>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89511879 | |||||||
| chr12:89512026 | C | T | 1 | a0001c0001t0004g0040 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.100+13094G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89512026 | |||||||
| chr12:89512037 | G | C | 3 | a0001c0001t0006g0226 a0001c0001t0006g0227 a0001c0001t0006g0228 |
3 | HG01070.hp2 HG01361.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.100+13083C>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89512037 | |||||||
| chr12:89512050 | T | C | 1 | a0001c0001t0002g0113 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.100+13070A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89512050 | |||||||
| chr12:89512236 | G | A | 1 | a0001c0001t0001g0011 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.100+12884C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89512236 | |||||||
| chr12:89512432 | T | C | 1 | a0001c0001t0001g0345 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.100+12688A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89512432 | |||||||
| chr12:89512452 | T | C | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(270): Show |
279 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(276): Show |
intron_variant | MODIFIER | c.100+12668A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89512452 | |||||||
| chr12:89512577 | A | G | 1 | a0002c0003t0001g0288 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.100+12543T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89512577 | |||||||
| chr12:89512611 | C | A | 6 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0003g0042 others(3): Show |
6 | HG02572.hp1 HG02615.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+12509G>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89512611 | |||||||
| chr12:89512689 | G | C | 1 | a0001c0001t0001g0011 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.100+12431C>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89512689 | |||||||
| chr12:89512933 | C | T | 1 | a0001c0001t0002g0163 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.100+12187G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89512933 | |||||||
| chr12:89513181 | T | C | 1 | a0001c0001t0001g0355 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.100+11939A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89513181 | |||||||
| chr12:89513219 | A | G | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+11901T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89513219 | |||||||
| chr12:89513233 | G | A | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(195): Show |
203 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.100+11887C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89513233 | |||||||
| chr12:89513250 | G | GA | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(196): Show |
204 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.100+11869dupT | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89513250 | |||||||
| chr12:89513250 | G | GAA | 25 | a0001c0001t0001g0004 a0001c0001t0001g0032 a0001c0001t0001g0097 others(22): Show |
26 | HG00408.hp2 HG01261.hp1 HG01993.hp1 others(23): Show |
intron_variant | MODIFIER | c.100+11868_100+1186 others(6): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89513250 | |||||||
| chr12:89513250 | GA | G | 6 | a0001c0001t0001g0116 a0001c0001t0002g0125 a0001c0001t0002g0126 others(3): Show |
6 | HG00408.hp1 HG00423.hp1 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+11869delT | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89513250 | |||||||
| chr12:89513347 | A | G | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+11773T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89513347 | |||||||
| chr12:89513389 | T | C | 76 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0230 others(73): Show |
77 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.100+11731A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89513389 | |||||||
| chr12:89513697 | T | C | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
195 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.100+11423A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89513697 | |||||||
| chr12:89513847 | T | A | 3 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0004g0284 |
3 | HG01167.hp2 HG01891.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.100+11273A>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89513847 | |||||||
| chr12:89514060 | G | A | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+11060C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89514060 | |||||||
| chr12:89514257 | T | C | 1 | a0001c0001t0001g0335 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.100+10863A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89514257 | |||||||
| chr12:89514298 | G | T | 1 | a0001c0001t0001g0214 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.100+10822C>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89514298 | |||||||
| chr12:89514402 | C | CT | 9 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0108 others(6): Show |
9 | HG00673.hp1 HG01167.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.100+10717dupA | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89514402 | |||||||
| chr12:89514402 | C | CTTTT | 15 | a0001c0001t0001g0098 a0001c0001t0001g0336 a0001c0001t0001g0337 others(12): Show |
15 | HG00323.hp2 HG00738.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.100+10714_100+1071 others(8): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89514402 | |||||||
| chr12:89514402 | C | CTTTTT | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(134): Show |
141 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.100+10713_100+1071 others(9): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89514402 | |||||||
| chr12:89514402 | C | CTTTTTT | 67 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(64): Show |
69 | HG00423.hp1 HG00639.hp1 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.100+10712_100+1071 others(10): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89514402 | |||||||
| chr12:89514402 | C | CTTTTTTT | 30 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0053 others(27): Show |
30 | HG00735.hp1 HG00741.hp2 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.100+10711_100+1071 others(11): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89514402 | |||||||
| chr12:89514402 | C | CTTTTTTT others(1): Show |
11 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0026 others(8): Show |
11 | HG00099.hp1 HG00621.hp1 HG00639.hp2 others(8): Show |
intron_variant | MODIFIER | c.100+10710_100+1071 others(12): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89514402 | |||||||
| chr12:89514402 | C | CTTTTTTT others(6): Show |
4 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0038 others(1): Show |
4 | HG01109.hp1 HG02976.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.100+10705_100+1071 others(17): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89514402 | |||||||
| chr12:89514402 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0001g0036 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.100+10704_100+1071 others(18): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89514402 | |||||||
| chr12:89514402 | CT | C | 6 | a0001c0001t0001g0046 a0001c0001t0001g0273 a0001c0001t0001g0274 others(3): Show |
6 | HG00323.hp1 HG00735.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+10717delA | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89514402 | |||||||
| chr12:89514402 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0204 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.100+10708_100+1071 others(14): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89514402 | |||||||
| chr12:89514441 | C | A | 274 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(271): Show |
280 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(277): Show |
intron_variant | MODIFIER | c.100+10679G>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89514441 | |||||||
| chr12:89514448 | G | C | 274 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(271): Show |
280 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(277): Show |
intron_variant | MODIFIER | c.100+10672C>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89514448 | |||||||
| chr12:89514502 | G | A | 3 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 |
3 | HG01192.hp1 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.100+10618C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89514502 | |||||||
| chr12:89514703 | C | T | 274 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(271): Show |
280 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(277): Show |
intron_variant | MODIFIER | c.100+10417G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89514703 | |||||||
| chr12:89514723 | T | C | 1 | a0001c0001t0001g0010 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.100+10397A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89514723 | |||||||
| chr12:89514850 | T | C | 278 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(275): Show |
284 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(281): Show |
intron_variant | MODIFIER | c.100+10270A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89514850 | |||||||
| chr12:89514914 | C | G | 274 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(271): Show |
280 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(277): Show |
intron_variant | MODIFIER | c.100+10206G>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89514914 | |||||||
| chr12:89514916 | C | T | 5 | a0001c0001t0005g0043 a0001c0001t0008g0359 a0001c0001t0008g0360 others(2): Show |
5 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.100+10204G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89514916 | |||||||
| chr12:89515196 | A | C | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+9924T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89515196 | |||||||
| chr12:89515207 | G | A | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(195): Show |
203 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.100+9913C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89515207 | |||||||
| chr12:89515240 | T | C | 3 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 |
3 | NA18989.hp2 NA18991.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.100+9880A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89515240 | |||||||
| chr12:89515285 | G | T | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
283 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.100+9835C>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89515285 | |||||||
| chr12:89515316 | G | T | 3 | a0001c0001t0002g0051 a0001c0001t0002g0114 a0001c0001t0002g0115 |
3 | NA18961.hp1 NA18998.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.100+9804C>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89515316 | |||||||
| chr12:89515376 | C | T | 8 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0036 others(5): Show |
8 | HG01109.hp1 HG01167.hp2 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.100+9744G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89515376 | |||||||
| chr12:89515440 | T | C | 3 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0004g0284 |
3 | HG01167.hp2 HG01891.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.100+9680A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89515440 | |||||||
| chr12:89515523 | G | A | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
283 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.100+9597C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89515523 | |||||||
| chr12:89515585 | G | A | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+9535C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89515585 | |||||||
| chr12:89515693 | G | A | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(270): Show |
279 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(276): Show |
intron_variant | MODIFIER | c.100+9427C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89515693 | |||||||
| chr12:89515764 | C | G | 63 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(60): Show |
66 | HG00423.hp2 HG00673.hp2 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.100+9356G>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89515764 | |||||||
| chr12:89515846 | A | G | 6 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0293 others(3): Show |
6 | HG00642.hp1 HG01261.hp1 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+9274T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89515846 | |||||||
| chr12:89515916 | C | T | 3 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0004g0284 |
3 | HG01167.hp2 HG01891.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.100+9204G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89515916 | |||||||
| chr12:89516058 | A | C | 15 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0192 others(12): Show |
15 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.100+9062T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89516058 | |||||||
| chr12:89516073 | T | C | 75 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0289 others(72): Show |
76 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.100+9047A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89516073 | |||||||
| chr12:89516119 | ACTCT | A | 3 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 |
3 | HG01192.hp1 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.100+8997_100+9000d others(6): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89516119 | |||||||
| chr12:89516140 | A | G | 6 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0003g0042 others(3): Show |
6 | HG02572.hp1 HG02615.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+8980T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89516140 | |||||||
| chr12:89516180 | C | T | 1 | a0001c0001t0001g0011 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.100+8940G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89516180 | |||||||
| chr12:89516443 | T | C | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(270): Show |
279 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(276): Show |
intron_variant | MODIFIER | c.100+8677A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89516443 | |||||||
| chr12:89516497 | C | T | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(270): Show |
279 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(276): Show |
intron_variant | MODIFIER | c.100+8623G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89516497 | |||||||
| chr12:89516520 | A | T | 1 | a0001c0001t0001g0060 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.100+8600T>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89516520 | |||||||
| chr12:89516521 | T | A | 1 | a0001c0001t0001g0060 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.100+8599A>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89516521 | |||||||
| chr12:89516522 | A | T | 1 | a0001c0001t0001g0060 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.100+8598T>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89516522 | |||||||
| chr12:89516560 | A | G | 1 | a0001c0001t0003g0350 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.100+8560T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89516560 | |||||||
| chr12:89516586 | A | G | 1 | a0001c0001t0001g0011 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.100+8534T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89516586 | |||||||
| chr12:89516601 | C | T | 2 | a0001c0001t0002g0112 a0001c0001t0002g0113 |
2 | HG02132.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.100+8519G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89516601 | |||||||
| chr12:89516680 | A | G | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | HG01346.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.100+8440T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89516680 | |||||||
| chr12:89516807 | T | C | 1 | a0001c0001t0001g0186 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.100+8313A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89516807 | |||||||
| chr12:89516856 | T | C | 1 | a0001c0001t0001g0187 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.100+8264A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89516856 | |||||||
| chr12:89516860 | C | T | 1 | a0001c0001t0001g0286 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.100+8260G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89516860 | |||||||
| chr12:89516903 | C | T | 1 | a0001c0001t0001g0229 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.100+8217G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89516903 | |||||||
| chr12:89516907 | G | A | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(277): Show |
286 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(283): Show |
intron_variant | MODIFIER | c.100+8213C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89516907 | |||||||
| chr12:89516994 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.100+8126G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89516994 | |||||||
| chr12:89517005 | G | A | 1 | a0001c0001t0004g0284 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.100+8115C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89517005 | |||||||
| chr12:89517050 | G | A | 18 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0192 others(15): Show |
18 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.100+8070C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89517050 | |||||||
| chr12:89517071 | AC | A | 4 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(1): Show |
4 | HG01109.hp1 HG02630.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.100+8048delG | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89517071 | |||||||
| chr12:89517294 | G | A | 1 | a0001c0001t0002g0169 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.100+7826C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89517294 | |||||||
| chr12:89517614 | C | T | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(277): Show |
286 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(283): Show |
intron_variant | MODIFIER | c.100+7506G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89517614 | |||||||
| chr12:89517724 | C | T | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
283 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.100+7396G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89517724 | |||||||
| chr12:89517953 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.100+7167G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89517953 | |||||||
| chr12:89517980 | C | A | 5 | a0001c0001t0002g0276 a0001c0001t0002g0279 a0001c0001t0007g0033 others(2): Show |
5 | HG02080.hp2 NA18959.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+7140G>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89517980 | |||||||
| chr12:89518116 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.100+7004T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89518116 | |||||||
| chr12:89518377 | T | C | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+6743A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89518377 | |||||||
| chr12:89518515 | A | G | 1 | a0001c0001t0002g0058 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.100+6605T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89518515 | |||||||
| chr12:89518537 | A | G | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+6583T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89518537 | |||||||
| chr12:89518568 | T | C | 67 | a0001c0001t0001g0103 a0001c0001t0001g0110 a0001c0001t0001g0111 others(64): Show |
67 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.100+6552A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89518568 | |||||||
| chr12:89518574 | CCAA | C | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(170): Show |
177 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.100+6543_100+6545d others(5): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89518574 | |||||||
| chr12:89518588 | A | G | 1 | a0001c0001t0001g0292 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.100+6532T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89518588 | |||||||
| chr12:89518614 | C | A | 66 | a0001c0001t0001g0103 a0001c0001t0001g0111 a0001c0001t0001g0116 others(63): Show |
66 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.100+6506G>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89518614 | |||||||
| chr12:89518795 | C | T | 5 | a0001c0001t0001g0029 a0001c0001t0001g0223 a0001c0001t0001g0224 others(2): Show |
5 | NA18945.hp1 NA18961.hp2 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.100+6325G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89518795 | |||||||
| chr12:89518907 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.100+6213A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89518907 | |||||||
| chr12:89519039 | T | C | 2 | a0001c0001t0001g0024 a0001c0001t0002g0189 |
2 | NA18978.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.100+6081A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89519039 | |||||||
| chr12:89519044 | C | T | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+6076G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89519044 | |||||||
| chr12:89519058 | G | A | 1 | a0001c0001t0001g0286 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.100+6062C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89519058 | |||||||
| chr12:89519132 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.100+5988G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89519132 | |||||||
| chr12:89519178 | A | T | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
283 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.100+5942T>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89519178 | |||||||
| chr12:89519546 | G | A | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
283 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.100+5574C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89519546 | |||||||
| chr12:89519642 | C | T | 75 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0289 others(72): Show |
76 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.100+5478G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89519642 | |||||||
| chr12:89519674 | GT | G | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+5445delA | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89519674 | |||||||
| chr12:89519718 | T | C | 1 | a0001c0001t0001g0280 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.100+5402A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89519718 | |||||||
| chr12:89519803 | A | AT | 272 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(269): Show |
278 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(275): Show |
intron_variant | MODIFIER | c.100+5316dupA | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89519803 | |||||||
| chr12:89519845 | T | C | 1 | a0002c0003t0001g0288 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.100+5275A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89519845 | |||||||
| chr12:89519856 | T | C | 19 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0191 others(16): Show |
19 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.100+5264A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89519856 | |||||||
| chr12:89520019 | G | A | 4 | a0001c0001t0001g0352 a0001c0001t0003g0350 a0001c0001t0003g0351 others(1): Show |
4 | HG02647.hp1 HG02922.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.100+5101C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89520019 | |||||||
| chr12:89520024 | T | C | 1 | a0001c0001t0001g0220 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.100+5096A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89520024 | |||||||
| chr12:89520132 | A | G | 1 | a0001c0001t0004g0040 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.100+4988T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89520132 | |||||||
| chr12:89520270 | A | C | 1 | a0001c0001t0001g0220 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.100+4850T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89520270 | |||||||
| chr12:89520365 | T | G | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
283 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.100+4755A>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89520365 | |||||||
| chr12:89520484 | T | C | 75 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0289 others(72): Show |
76 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.100+4636A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89520484 | |||||||
| chr12:89520826 | G | A | 1 | a0001c0001t0001g0007 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.100+4294C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89520826 | |||||||
| chr12:89521098 | A | AT | 9 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(6): Show |
10 | HG00741.hp2 HG01361.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.100+4021dupA | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89521098 | |||||||
| chr12:89521098 | A | ATT | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+4020_100+4021d others(4): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89521098 | |||||||
| chr12:89521101 | TTA | T | 6 | a0001c0001t0001g0035 a0001c0001t0001g0170 a0001c0001t0001g0290 others(3): Show |
6 | HG02735.hp2 HG02976.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.100+4017_100+4018d others(4): Show |
POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89521101 | |||||||
| chr12:89521102 | TA | T | 191 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(188): Show |
194 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.100+4017delT | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89521102 | |||||||
| chr12:89521103 | A | T | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(77): Show |
83 | HG00423.hp2 HG00673.hp2 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.100+4017T>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89521103 | |||||||
| chr12:89521105 | T | A | 1 | a0001c0001t0001g0024 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.100+4015A>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89521105 | |||||||
| chr12:89521106 | A | T | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
283 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.100+4014T>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89521106 | |||||||
| chr12:89521109 | A | T | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
283 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.100+4011T>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89521109 | |||||||
| chr12:89521112 | T | A | 1 | a0001c0001t0001g0281 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.100+4008A>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89521112 | |||||||
| chr12:89521528 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.100+3592C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89521528 | |||||||
| chr12:89521537 | G | A | 3 | a0001c0001t0005g0043 a0001c0001t0005g0044 a0001c0001t0005g0045 |
3 | HG02615.hp1 HG03540.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.100+3583C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89521537 | |||||||
| chr12:89521553 | T | C | 4 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(1): Show |
4 | HG01109.hp1 HG02630.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.100+3567A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89521553 | |||||||
| chr12:89521604 | C | T | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+3516G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89521604 | |||||||
| chr12:89521772 | C | G | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
283 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.100+3348G>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89521772 | |||||||
| chr12:89521853 | G | C | 1 | a0001c0001t0001g0011 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.100+3267C>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89521853 | |||||||
| chr12:89521945 | T | C | 25 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0023 others(22): Show |
26 | HG00621.hp1 HG00733.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.100+3175A>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89521945 | |||||||
| chr12:89522098 | A | G | 5 | a0001c0001t0001g0004 a0001c0001t0001g0104 a0001c0001t0001g0105 others(2): Show |
6 | HG02486.hp1 HG02723.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+3022T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89522098 | |||||||
| chr12:89522129 | G | A | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | HG01346.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.100+2991C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89522129 | |||||||
| chr12:89522152 | A | G | 6 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(3): Show |
6 | HG00673.hp1 HG02165.hp1 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+2968T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89522152 | |||||||
| chr12:89522455 | A | C | 1 | a0001c0001t0001g0047 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.100+2665T>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89522455 | |||||||
| chr12:89522888 | C | T | 7 | a0001c0001t0001g0028 a0001c0001t0001g0209 a0001c0001t0001g0210 others(4): Show |
7 | HG01243.hp1 HG02559.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.100+2232G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89522888 | |||||||
| chr12:89522895 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.100+2225G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89522895 | |||||||
| chr12:89523034 | C | T | 63 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(60): Show |
66 | HG00423.hp2 HG00673.hp2 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.100+2086G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89523034 | |||||||
| chr12:89523077 | G | T | 1 | a0001c0001t0001g0289 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.100+2043C>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89523077 | |||||||
| chr12:89523191 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.100+1929C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89523191 | |||||||
| chr12:89523198 | C | G | 1 | a0001c0001t0001g0052 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.100+1922G>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89523198 | |||||||
| chr12:89523247 | A | T | 1 | a0001c0001t0002g0051 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.100+1873T>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89523247 | |||||||
| chr12:89523260 | G | A | 19 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0191 others(16): Show |
19 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.100+1860C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89523260 | |||||||
| chr12:89523453 | T | G | 1 | a0001c0001t0002g0208 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.100+1667A>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89523453 | |||||||
| chr12:89523524 | A | G | 1 | a0001c0001t0001g0027 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.100+1596T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89523524 | |||||||
| chr12:89523588 | A | T | 1 | a0002c0003t0001g0288 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.100+1532T>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89523588 | |||||||
| chr12:89523741 | A | G | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
283 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.100+1379T>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89523741 | |||||||
| chr12:89523849 | G | T | 4 | a0001c0001t0008g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 others(1): Show |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+1271C>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89523849 | |||||||
| chr12:89523920 | G | A | 1 | a0001c0001t0002g0282 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.100+1200C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89523920 | |||||||
| chr12:89524571 | G | A | 1 | a0001c0001t0001g0283 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.100+549C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89524571 | |||||||
| chr12:89524622 | G | A | 1 | a0001c0001t0004g0284 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.100+498C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89524622 | |||||||
| chr12:89524818 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.100+302G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89524818 | |||||||
| chr12:89524829 | G | A | 1 | a0001c0001t0001g0285 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.100+291C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89524829 | |||||||
| chr12:89524900 | C | A | 75 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0289 others(72): Show |
76 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.100+220G>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89524900 | |||||||
| chr12:89524923 | G | A | 1 | a0001c0001t0001g0286 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.100+197C>T | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89524923 | |||||||
| chr12:89524994 | C | T | 1 | a0001c0001t0001g0050 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.100+126G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89524994 | |||||||
| chr12:89525072 | C | T | 3 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 |
3 | HG01192.hp1 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.100+48G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 2/11 | chr12 | 89525072 | |||||||
| chr12:89525551 | C | CT | 80 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(77): Show |
81 | HG00323.hp2 HG00597.hp2 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.15+329dupA | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 1/11 | chr12 | 89525551 | |||||||
| chr12:89525611 | C | G | 1 | a0001c0001t0004g0287 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.15+270G>C | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 1/11 | chr12 | 89525611 | |||||||
| chr12:89525665 | G | C | 4 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(1): Show |
4 | HG01109.hp1 HG02630.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+216C>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 1/11 | chr12 | 89525665 | |||||||
| chr12:89525741 | C | T | 4 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(1): Show |
4 | HG01109.hp1 HG02630.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+140G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 1/11 | chr12 | 89525741 | |||||||
| chr12:89525752 | G | C | 2 | a0001c0001t0009g0008 a0001c0001t0009g0009 |
2 | HG02647.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.15+129C>G | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 1/11 | chr12 | 89525752 | |||||||
| chr12:89525791 | C | T | 75 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0289 others(72): Show |
76 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.15+90G>A | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 1/11 | chr12 | 89525791 | |||||||
| chr12:89525853 | A | AC | 24 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(21): Show |
24 | HG00597.hp1 HG00621.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.15+27dupG | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 1/11 | chr12 | 89525853 | |||||||
| chr12:89525853 | ACC | A | 78 | a0001c0001t0001g0007 a0001c0001t0001g0289 a0001c0001t0001g0290 others(75): Show |
79 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.15+26_15+27delGG | POC1B | ENSG00000139323.14 | transcript | ENST00000313546.8 | protein_coding | 1/11 | chr12 | 89525853 |