Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 57097 |
|---|---|
| ensemblid | ENSG00000111224.14 |
| hgncid | 1186 |
| symbol | PARP11 |
| name | poly(ADP-ribose) polymerase family member 11 |
| refseq_nuc | NM_020367.6 |
| refseq_prot | NP_065100.2 |
| ensembl_nuc | ENST00000228820.9 |
| ensembl_prot | ENSP00000228820.4 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 3808861 |
| end | 3873399 |
| strand | - |
| ver | v1.2 |
| region | chr12:3808861-3873399 |
| region5000 | chr12:3803861-3878399 |
| regionname0 | PARP11_chr12_3808861_3873399 |
| regionname5000 | PARP11_chr12_3803861_3878399 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 338 | 416 | 92 | 68 | 200 | 10 | 44 | 154 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 3412 | 45 | 9 | 0 | 33 | 0 | 3 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0002 | 0/0 | 3430 | 43 | 4 | 8 | 27 | 0 | 4 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0003 | 0/0 | 3430 | 41 | 1 | 5 | 35 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0004 | 0/0 | 3434 | 36 | 2 | 12 | 13 | 3 | 6 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0005 | 0/0 | 3440 | 36 | 11 | 9 | 8 | 2 | 6 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0006 | 0/0 | 3443 | 25 | 2 | 0 | 18 | 0 | 5 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0007 | 0/0 | 3450 | 18 | 0 | 0 | 18 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0008 | 0/0 | 3426 | 16 | 13 | 1 | 0 | 0 | 2 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0009 | 0/0 | 3432 | 12 | 12 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0010 | 0/0 | 3426 | 11 | 2 | 1 | 3 | 2 | 3 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0011 | 0/1 | 3437 | 10 | 2 | 0 | 3 | 1 | 3 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0012 | 0/0 | 3430 | 6 | 0 | 5 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0013 | 0/0 | 3444 | 6 | 1 | 5 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0014 | 0/0 | 3433 | 6 | 3 | 2 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0015 | 0/0 | 3431 | 6 | 5 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0016 | 0/0 | 3437 | 6 | 0 | 0 | 6 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0017 | 0/0 | 3424 | 4 | 0 | 2 | 0 | 0 | 2 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0018 | 0/0 | 3454 | 4 | 0 | 0 | 4 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0019 | 0/0 | 3443 | 4 | 3 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0020 | 0/0 | 3434 | 3 | 0 | 2 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0021 | 0/0 | 3435 | 3 | 0 | 2 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0022 | 0/0 | 3450 | 3 | 0 | 0 | 3 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0023 | 0/0 | 3420 | 3 | 0 | 0 | 2 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0024 | 0/0 | 3430 | 2 | 0 | 1 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0025 | 0/0 | 3426 | 2 | 0 | 2 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0026 | 0/0 | 3413 | 2 | 0 | 0 | 2 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0027 | 0/0 | 3441 | 2 | 0 | 1 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0028 | 0/0 | 3443 | 2 | 0 | 2 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0029 | 0/0 | 3406 | 2 | 0 | 1 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0030 | 0/0 | 3440 | 2 | 0 | 2 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0031 | 0/0 | 3458 | 2 | 0 | 0 | 2 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0032 | 0/0 | 3446 | 2 | 0 | 0 | 2 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0033 | 0/0 | 3452 | 2 | 2 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0034 | 0/0 | 3446 | 2 | 2 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0035 | 0/0 | 3430 | 2 | 0 | 0 | 2 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0036 | 0/0 | 3439 | 2 | 2 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0037 | 0/0 | 3428 | 1 | 0 | 0 | 0 | 1 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0038 | 0/0 | 3416 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0039 | 0/0 | 3411 | 1 | 0 | 0 | 0 | 1 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0040 | 0/0 | 3426 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0041 | 0/0 | 3437 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0042 | 0/0 | 3440 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0043 | 0/0 | 3438 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0044 | 0/0 | 3431 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0045 | 0/0 | 3451 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0046 | 0/0 | 3452 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0047 | 0/0 | 3434 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0048 | 0/0 | 3454 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0049 | 0/0 | 3442 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0050 | 0/0 | 3434 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0051 | 0/0 | 3435 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0052 | 0/0 | 3424 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0053 | 0/0 | 3413 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0054 | 0/0 | 3441 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0055 | 0/0 | 3437 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0056 | 0/0 | 3438 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0057 | 0/0 | 3438 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0058 | 0/0 | 3437 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0059 | 0/0 | 3434 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0060 | 1/0 | 3433 | 1 | 0 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0061 | 0/0 | 3434 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0062 | 0/0 | 3450 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0063 | 0/0 | 3446 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0064 | 0/0 | 3456 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0065 | 0/0 | 3448 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0066 | 0/0 | 3447 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0067 | 0/0 | 3427 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0068 | 0/0 | 3426 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0069 | 0/0 | 3440 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0070 | 0/0 | 3446 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0071 | 0/0 | 3446 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0072 | 0/0 | 3432 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0073 | 0/0 | 3440 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0074 | 0/0 | 3446 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0075 | 0/0 | 3441 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0076 | 0/0 | 3430 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0077 | 0/0 | 3430 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0078 | 0/0 | 3430 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| t0079 | 0/0 | 3430 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 12 | 0 | 4 | 8 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0002 | 0/0 | 12 | 0 | 0 | 11 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0003 | 0/0 | 8 | 0 | 3 | 3 | 1 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0005 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0006 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0007 | 0/0 | 5 | 0 | 0 | 2 | 1 | 2 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0010 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0011 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0012 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0016 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0021 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0022 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0024 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0033 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0034 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0049 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0052 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0053 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0264 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0290 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1017 | 415 | 92 | 68 | 199 | 10 | 44 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0002 | 0/0 | 1017 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4428 | 45 | 9 | 0 | 33 | 0 | 3 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0002 | 0/0 | 4446 | 43 | 4 | 8 | 27 | 0 | 4 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0003 | 0/0 | 4446 | 40 | 1 | 5 | 34 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0004 | 0/0 | 4450 | 36 | 2 | 12 | 13 | 3 | 6 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0005 | 0/0 | 4456 | 36 | 11 | 9 | 8 | 2 | 6 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0006 | 0/0 | 4459 | 25 | 2 | 0 | 18 | 0 | 5 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0007 | 0/0 | 4466 | 18 | 0 | 0 | 18 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0008 | 0/0 | 4442 | 16 | 13 | 1 | 0 | 0 | 2 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0009 | 0/0 | 4448 | 12 | 12 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0010 | 0/0 | 4442 | 11 | 2 | 1 | 3 | 2 | 3 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0011 | 0/1 | 4453 | 10 | 2 | 0 | 3 | 1 | 3 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0012 | 0/0 | 4446 | 6 | 0 | 5 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0013 | 0/0 | 4460 | 6 | 1 | 5 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0014 | 0/0 | 4449 | 6 | 3 | 2 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0015 | 0/0 | 4447 | 6 | 5 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0016 | 0/0 | 4453 | 6 | 0 | 0 | 6 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0017 | 0/0 | 4440 | 4 | 0 | 2 | 0 | 0 | 2 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0018 | 0/0 | 4470 | 4 | 0 | 0 | 4 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0019 | 0/0 | 4459 | 4 | 3 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0020 | 0/0 | 4450 | 3 | 0 | 2 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0021 | 0/0 | 4451 | 3 | 0 | 2 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0022 | 0/0 | 4466 | 3 | 0 | 0 | 3 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0023 | 0/0 | 4436 | 3 | 0 | 0 | 2 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0024 | 0/0 | 4446 | 2 | 0 | 1 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0025 | 0/0 | 4442 | 2 | 0 | 2 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0026 | 0/0 | 4429 | 2 | 0 | 0 | 2 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0027 | 0/0 | 4457 | 2 | 0 | 1 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0028 | 0/0 | 4459 | 2 | 0 | 2 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0029 | 0/0 | 4422 | 2 | 0 | 1 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0030 | 0/0 | 4456 | 2 | 0 | 2 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0031 | 0/0 | 4474 | 2 | 0 | 0 | 2 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0032 | 0/0 | 4462 | 2 | 0 | 0 | 2 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0033 | 0/0 | 4468 | 2 | 2 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0034 | 0/0 | 4462 | 2 | 2 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0035 | 0/0 | 4446 | 2 | 0 | 0 | 2 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0036 | 0/0 | 4455 | 2 | 2 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0037 | 0/0 | 4444 | 1 | 0 | 0 | 0 | 1 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0038 | 0/0 | 4432 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0039 | 0/0 | 4427 | 1 | 0 | 0 | 0 | 1 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0040 | 0/0 | 4442 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0041 | 0/0 | 4453 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0042 | 0/0 | 4456 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0043 | 0/0 | 4454 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0044 | 0/0 | 4447 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0045 | 0/0 | 4467 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0046 | 0/0 | 4468 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0047 | 0/0 | 4450 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0048 | 0/0 | 4470 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0049 | 0/0 | 4458 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0050 | 0/0 | 4450 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0051 | 0/0 | 4451 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0052 | 0/0 | 4440 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0053 | 0/0 | 4429 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0054 | 0/0 | 4457 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0055 | 0/0 | 4453 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0056 | 0/0 | 4454 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0057 | 0/0 | 4454 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0058 | 0/0 | 4453 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0059 | 0/0 | 4450 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0060 | 1/0 | 4449 | 1 | 0 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0061 | 0/0 | 4450 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0062 | 0/0 | 4466 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0063 | 0/0 | 4462 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0064 | 0/0 | 4472 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0065 | 0/0 | 4464 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0066 | 0/0 | 4463 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0067 | 0/0 | 4443 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0068 | 0/0 | 4442 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0069 | 0/0 | 4456 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0070 | 0/0 | 4462 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0071 | 0/0 | 4462 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0072 | 0/0 | 4448 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0073 | 0/0 | 4456 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0074 | 0/0 | 4462 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0075 | 0/0 | 4457 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0076 | 0/0 | 4446 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0077 | 0/0 | 4446 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0078 | 0/0 | 4446 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0001t0079 | 0/0 | 4446 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| a0001c0002t0003 | 0/0 | 4446 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | copy fasta | chr12 | 3803861 | 3878399 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 12 | 0 | 0 | 11 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0001g0005 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0002g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0002g0022 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0002g0024 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0002g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0002g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0002g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0003g0001 | 0/0 | 12 | 0 | 4 | 8 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0003g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0003g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0003g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0003g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0004g0007 | 0/0 | 5 | 0 | 0 | 2 | 1 | 2 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0004g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0004g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0004g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0004g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0004g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0004g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0004g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0004g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0004g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0004g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0004g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0004g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0004g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0004g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0004g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0004g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0004g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0004g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0004g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0004g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0005g0003 | 0/0 | 8 | 0 | 3 | 3 | 1 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0005g0033 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0005g0034 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0005g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0005g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0005g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0005g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0005g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0005g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0005g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0005g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0005g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0005g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0005g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0005g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0005g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0005g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0005g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0005g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0005g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0005g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0005g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0005g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0006g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0006g0021 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0006g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0006g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0006g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0006g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0006g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0006g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0006g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0006g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0006g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0006g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0006g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0006g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0006g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0006g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0006g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0007g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0007g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0007g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0007g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0007g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0007g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0007g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0007g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0007g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0007g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0007g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0007g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0007g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0008g0016 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0008g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0008g0052 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0008g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0008g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0008g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0008g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0008g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0008g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0008g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0008g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0009g0006 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0009g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0009g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0009g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0009g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0009g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0009g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0010g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0010g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0010g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0010g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0010g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0010g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0010g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0010g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0010g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0010g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0011g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0011g0049 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0011g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0011g0264 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0011g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0011g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0011g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0011g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0012g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0012g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0012g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0012g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0012g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0013g0011 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0013g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0013g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0014g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0014g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0014g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0014g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0014g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0014g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0015g0012 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0015g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0016g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0016g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0017g0010 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0018g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0018g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0018g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0018g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0019g0053 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0019g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0019g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0020g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0020g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0020g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0021g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0021g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0021g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0022g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0022g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0022g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0023g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0023g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0023g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0024g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0025g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0025g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0026g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0027g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0027g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0028g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0029g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0029g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0030g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0031g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0031g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0032g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0032g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0033g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0034g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0034g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0035g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0035g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0036g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0036g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0037g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0038g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0039g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0040g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0041g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0042g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0043g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0044g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0045g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0046g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0047g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0048g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0049g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0050g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0051g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0052g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0053g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0054g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0055g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0056g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0057g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0058g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0059g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0060g0290 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0061g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0062g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0063g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0064g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0065g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0066g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0067g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0068g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0069g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0070g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0071g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0072g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0073g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0074g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0075g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0076g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0077g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0078g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0079g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0002t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0242 | EUR | GBR | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0282 | EUR | GBR | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG00323 | hp1 | a0001 | c0001 | t0037 | g0054 | EUR | FIN | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG00323 | hp2 | a0001 | c0001 | t0011 | g0049 | EUR | FIN | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG00408 | hp1 | a0001 | c0001 | t0067 | g0222 | EAS | CHS | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG00408 | hp2 | a0001 | c0001 | t0004 | g0258 | EAS | CHS | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | CHS | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG00423 | hp2 | a0001 | c0001 | t0011 | g0265 | EAS | CHS | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG00438 | hp1 | a0001 | c0001 | t0043 | g0085 | EAS | CHS | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | CHS | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG00544 | hp2 | a0001 | c0001 | t0058 | g0220 | EAS | CHS | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | CHS | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | CHS | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG00597 | hp2 | a0001 | c0001 | t0004 | g0233 | EAS | CHS | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG00609 | hp1 | a0001 | c0001 | t0011 | g0048 | EAS | CHS | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG00621 | hp1 | a0001 | c0001 | t0016 | g0008 | EAS | CHS | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | CHS | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0238 | AMR | PUR | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG00639 | hp2 | a0001 | c0001 | t0027 | g0079 | AMR | PUR | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG00642 | hp1 | a0001 | c0001 | t0017 | g0010 | AMR | PUR | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG00642 | hp2 | a0001 | c0001 | t0004 | g0254 | AMR | PUR | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0250 | AMR | PUR | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG00735 | hp2 | a0001 | c0001 | t0020 | g0063 | AMR | PUR | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG00738 | hp1 | a0001 | c0001 | t0020 | g0062 | AMR | PUR | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG00741 | hp1 | a0001 | c0001 | t0010 | g0073 | AMR | PUR | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG00741 | hp2 | a0001 | c0001 | t0012 | g0061 | AMR | PUR | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01069 | hp2 | a0001 | c0001 | t0061 | g0235 | AMR | PUR | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0160 | AMR | PUR | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0232 | AMR | PUR | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01074 | hp2 | a0001 | c0001 | t0004 | g0260 | AMR | PUR | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01081 | hp1 | a0001 | c0001 | t0005 | g0003 | AMR | PUR | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01081 | hp2 | a0001 | c0001 | t0047 | g0253 | AMR | PUR | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01106 | hp1 | a0001 | c0001 | t0013 | g0011 | AMR | PUR | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01106 | hp2 | a0001 | c0001 | t0005 | g0175 | AMR | PUR | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01109 | hp1 | a0001 | c0001 | t0029 | g0134 | AMR | PUR | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01109 | hp2 | a0001 | c0001 | t0012 | g0026 | AMR | PUR | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0239 | AMR | PUR | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01168 | hp2 | a0001 | c0001 | t0017 | g0010 | AMR | PUR | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01169 | hp1 | a0001 | c0001 | t0008 | g0016 | AMR | PUR | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | PUR | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01175 | hp1 | a0001 | c0001 | t0021 | g0083 | AMR | PUR | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0289 | AMR | PUR | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01192 | hp1 | a0001 | c0001 | t0014 | g0169 | AMR | PUR | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01243 | hp1 | a0001 | c0001 | t0012 | g0067 | AMR | PUR | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0283 | AMR | PUR | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01255 | hp1 | a0001 | c0001 | t0005 | g0033 | AMR | CLM | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01255 | hp2 | a0001 | c0001 | t0025 | g0068 | AMR | CLM | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0259 | AMR | CLM | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01256 | hp2 | a0001 | c0001 | t0005 | g0228 | AMR | CLM | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01257 | hp1 | a0001 | c0001 | t0025 | g0070 | AMR | CLM | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01257 | hp2 | a0001 | c0001 | t0004 | g0244 | AMR | CLM | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01261 | hp1 | a0001 | c0001 | t0021 | g0082 | AMR | CLM | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01261 | hp2 | a0001 | c0001 | t0028 | g0035 | AMR | CLM | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01346 | hp1 | a0001 | c0001 | t0019 | g0053 | AMR | CLM | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01346 | hp2 | a0001 | c0001 | t0004 | g0236 | AMR | CLM | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01358 | hp1 | a0001 | c0001 | t0028 | g0035 | AMR | CLM | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01358 | hp2 | a0001 | c0001 | t0014 | g0183 | AMR | CLM | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01433 | hp1 | a0001 | c0001 | t0024 | g0025 | AMR | CLM | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0252 | AMR | CLM | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01496 | hp1 | a0001 | c0001 | t0030 | g0038 | AMR | CLM | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01496 | hp2 | a0001 | c0001 | t0005 | g0170 | AMR | CLM | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01515 | hp1 | a0001 | c0001 | t0010 | g0074 | EUR | IBS | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01515 | hp2 | a0001 | c0001 | t0005 | g0033 | EUR | IBS | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01884 | hp1 | a0001 | c0001 | t0009 | g0006 | AFR | ACB | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01884 | hp2 | a0001 | c0001 | t0005 | g0041 | AFR | ACB | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01891 | hp1 | a0001 | c0001 | t0072 | g0154 | AFR | ACB | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01891 | hp2 | a0001 | c0001 | t0051 | g0167 | AFR | ACB | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01934 | hp1 | a0001 | c0001 | t0030 | g0038 | AMR | PEL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01934 | hp2 | a0001 | c0001 | t0059 | g0241 | AMR | PEL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01952 | hp1 | a0001 | c0001 | t0005 | g0034 | AMR | PEL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01952 | hp2 | a0001 | c0001 | t0015 | g0012 | AMR | PEL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01975 | hp1 | a0001 | c0001 | t0005 | g0003 | AMR | PEL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01975 | hp2 | a0001 | c0001 | t0013 | g0011 | AMR | PEL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01981 | hp1 | a0001 | c0001 | t0013 | g0203 | AMR | PEL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01981 | hp2 | a0001 | c0001 | t0012 | g0057 | AMR | PEL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01993 | hp1 | a0001 | c0001 | t0004 | g0257 | AMR | PEL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01993 | hp2 | a0001 | c0001 | t0013 | g0011 | AMR | PEL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02004 | hp1 | a0001 | c0001 | t0005 | g0184 | AMR | PEL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0029 | AMR | PEL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02015 | hp1 | a0001 | c0001 | t0007 | g0036 | EAS | KHV | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02015 | hp2 | a0001 | c0001 | t0077 | g0093 | EAS | KHV | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02027 | hp1 | a0001 | c0001 | t0007 | g0201 | EAS | KHV | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02027 | hp2 | a0001 | c0001 | t0074 | g0174 | EAS | KHV | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02040 | hp1 | a0001 | c0001 | t0004 | g0046 | EAS | KHV | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | KHV | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02055 | hp1 | a0001 | c0001 | t0008 | g0115 | AFR | ACB | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02055 | hp2 | a0001 | c0001 | t0050 | g0140 | AFR | ACB | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02056 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | KHV | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02056 | hp2 | a0001 | c0001 | t0007 | g0037 | EAS | KHV | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02074 | hp2 | a0001 | c0001 | t0049 | g0186 | EAS | KHV | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02080 | hp1 | a0001 | c0001 | t0004 | g0046 | EAS | KHV | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02129 | hp1 | a0001 | c0001 | t0007 | g0039 | EAS | KHV | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | KHV | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0105 | EAS | KHV | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02132 | hp2 | a0001 | c0001 | t0048 | g0189 | EAS | KHV | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | KHV | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02135 | hp2 | a0001 | c0001 | t0006 | g0215 | EAS | KHV | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02148 | hp1 | a0001 | c0001 | t0004 | g0231 | AMR | PEL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02148 | hp2 | a0001 | c0001 | t0013 | g0011 | AMR | PEL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | CDX | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02155 | hp2 | a0001 | c0001 | t0022 | g0185 | EAS | CDX | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02165 | hp1 | a0001 | c0001 | t0010 | g0027 | EAS | CDX | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0094 | EAS | CDX | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02257 | hp1 | a0001 | c0001 | t0005 | g0041 | AFR | ACB | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0240 | AFR | ACB | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02258 | hp2 | a0001 | c0001 | t0015 | g0012 | AFR | ACB | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02273 | hp2 | a0001 | c0001 | t0012 | g0026 | AMR | PEL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02280 | hp1 | a0001 | c0001 | t0036 | g0300 | AFR | ACB | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02280 | hp2 | a0001 | c0001 | t0005 | g0040 | AFR | ACB | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02300 | hp1 | a0001 | c0001 | t0004 | g0249 | AMR | PEL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02300 | hp2 | a0001 | c0001 | t0005 | g0003 | AMR | PEL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02451 | hp2 | a0001 | c0001 | t0068 | g0156 | AFR | ACB | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02523 | hp1 | a0001 | c0001 | t0054 | g0263 | EAS | KHV | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0091 | EAS | KHV | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02602 | hp1 | a0001 | c0001 | t0038 | g0055 | SAS | PJL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02602 | hp2 | a0001 | c0001 | t0004 | g0251 | SAS | PJL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02615 | hp1 | a0001 | c0001 | t0011 | g0168 | AFR | GWD | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02615 | hp2 | a0001 | c0001 | t0069 | g0147 | AFR | GWD | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02622 | hp1 | a0001 | c0001 | t0033 | g0044 | AFR | GWD | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02622 | hp2 | a0001 | c0001 | t0034 | g0136 | AFR | GWD | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0100 | AFR | GWD | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02630 | hp2 | a0001 | c0001 | t0010 | g0066 | AFR | GWD | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02647 | hp1 | a0001 | c0001 | t0010 | g0065 | AFR | GWD | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02647 | hp2 | a0001 | c0001 | t0008 | g0279 | AFR | GWD | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02683 | hp1 | a0001 | c0001 | t0004 | g0243 | SAS | PJL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02683 | hp2 | a0001 | c0001 | t0006 | g0226 | SAS | PJL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02698 | hp1 | a0001 | c0001 | t0010 | g0072 | SAS | PJL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02698 | hp2 | a0001 | c0001 | t0041 | g0060 | SAS | PJL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02717 | hp1 | a0001 | c0001 | t0006 | g0216 | AFR | GWD | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02717 | hp2 | a0001 | c0001 | t0019 | g0053 | AFR | GWD | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0210 | AFR | GWD | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02723 | hp2 | a0001 | c0001 | t0009 | g0159 | AFR | GWD | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02735 | hp1 | a0001 | c0001 | t0029 | g0120 | SAS | PJL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02735 | hp2 | a0001 | c0001 | t0040 | g0077 | SAS | PJL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02738 | hp1 | a0001 | c0001 | t0004 | g0261 | SAS | PJL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02738 | hp2 | a0001 | c0001 | t0010 | g0075 | SAS | PJL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02809 | hp1 | a0001 | c0001 | t0009 | g0155 | AFR | GWD | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02818 | hp1 | a0001 | c0001 | t0071 | g0230 | AFR | GWD | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0042 | AFR | GWD | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02886 | hp1 | a0001 | c0001 | t0008 | g0130 | AFR | GWD | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02886 | hp2 | a0001 | c0001 | t0006 | g0217 | AFR | GWD | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02895 | hp1 | a0001 | c0001 | t0008 | g0108 | AFR | GWD | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02895 | hp2 | a0001 | c0001 | t0009 | g0006 | AFR | GWD | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0138 | AFR | GWD | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02897 | hp1 | a0001 | c0001 | t0009 | g0006 | AFR | GWD | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02922 | hp2 | a0001 | c0001 | t0042 | g0058 | AFR | ESN | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02965 | hp1 | a0001 | c0001 | t0009 | g0153 | AFR | ESN | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02965 | hp2 | a0001 | c0001 | t0009 | g0006 | AFR | ESN | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0043 | AFR | ESN | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02970 | hp2 | a0001 | c0001 | t0009 | g0032 | AFR | ESN | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0209 | AFR | ESN | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02976 | hp2 | a0001 | c0001 | t0065 | g0212 | AFR | ESN | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG03017 | hp1 | a0001 | c0001 | t0055 | g0266 | SAS | PJL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0281 | SAS | PJL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG03041 | hp1 | a0001 | c0001 | t0064 | g0211 | AFR | GWD | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG03041 | hp2 | a0001 | c0001 | t0008 | g0016 | AFR | GWD | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG03130 | hp1 | a0001 | c0001 | t0015 | g0030 | AFR | ESN | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG03130 | hp2 | a0001 | c0001 | t0019 | g0299 | AFR | ESN | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG03139 | hp1 | a0001 | c0001 | t0014 | g0118 | AFR | ESN | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG03139 | hp2 | a0001 | c0001 | t0008 | g0018 | AFR | ESN | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG03195 | hp1 | a0001 | c0001 | t0009 | g0158 | AFR | ESN | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG03195 | hp2 | a0001 | c0001 | t0009 | g0032 | AFR | ESN | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG03209 | hp1 | a0001 | c0001 | t0015 | g0012 | AFR | MSL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG03209 | hp2 | a0001 | c0001 | t0063 | g0148 | AFR | MSL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG03225 | hp1 | a0001 | c0001 | t0073 | g0173 | AFR | MSL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG03225 | hp2 | a0001 | c0001 | t0008 | g0295 | AFR | MSL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG03239 | hp1 | a0001 | c0001 | t0005 | g0143 | SAS | PJL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0285 | SAS | PJL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG03453 | hp1 | a0001 | c0001 | t0008 | g0131 | AFR | MSL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG03453 | hp2 | a0001 | c0001 | t0070 | g0139 | AFR | MSL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG03486 | hp1 | a0001 | c0001 | t0014 | g0166 | AFR | MSL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG03486 | hp2 | a0001 | c0001 | t0008 | g0109 | AFR | MSL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG03491 | hp1 | a0001 | c0001 | t0005 | g0176 | SAS | PJL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0007 | SAS | PJL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG03516 | hp1 | a0001 | c0001 | t0008 | g0018 | AFR | ESN | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG03516 | hp2 | a0001 | c0001 | t0015 | g0030 | AFR | ESN | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG03540 | hp1 | a0001 | c0001 | t0033 | g0044 | AFR | GWD | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG03579 | hp1 | a0001 | c0001 | t0034 | g0137 | AFR | MSL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG03579 | hp2 | a0001 | c0001 | t0008 | g0016 | AFR | MSL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG03654 | hp1 | a0001 | c0001 | t0017 | g0010 | SAS | PJL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG03654 | hp2 | a0001 | c0001 | t0011 | g0270 | SAS | PJL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG03669 | hp1 | a0001 | c0001 | t0010 | g0059 | SAS | PJL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG03669 | hp2 | a0001 | c0001 | t0005 | g0180 | SAS | PJL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG03688 | hp1 | a0001 | c0001 | t0008 | g0052 | SAS | STU | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG03688 | hp2 | a0001 | c0001 | t0005 | g0144 | SAS | STU | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG03704 | hp2 | a0001 | c0001 | t0017 | g0010 | SAS | PJL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0007 | SAS | PJL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG03710 | hp2 | a0001 | c0001 | t0020 | g0069 | SAS | PJL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG03831 | hp1 | a0001 | c0001 | t0011 | g0271 | SAS | BEB | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG03834 | hp1 | a0001 | c0001 | t0012 | g0076 | SAS | BEB | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG03834 | hp2 | a0001 | c0001 | t0011 | g0272 | SAS | BEB | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG03927 | hp1 | a0001 | c0001 | t0005 | g0179 | SAS | BEB | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG03927 | hp2 | a0001 | c0001 | t0006 | g0218 | SAS | BEB | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG04115 | hp1 | a0001 | c0001 | t0006 | g0227 | SAS | STU | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG04115 | hp2 | a0001 | c0001 | t0004 | g0255 | SAS | STU | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG04184 | hp1 | a0001 | c0001 | t0014 | g0267 | SAS | BEB | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG04184 | hp2 | a0001 | c0001 | t0006 | g0021 | SAS | BEB | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0287 | SAS | STU | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | STU | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG04204 | hp1 | a0001 | c0001 | t0046 | g0081 | SAS | STU | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG04204 | hp2 | a0001 | c0001 | t0023 | g0161 | SAS | STU | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG04228 | hp1 | a0001 | c0001 | t0008 | g0052 | SAS | STU | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0273 | SAS | STU | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18522 | hp1 | a0001 | c0001 | t0019 | g0297 | AFR | YRI | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18522 | hp2 | a0001 | c0001 | t0014 | g0165 | AFR | YRI | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CHB | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18612 | hp2 | a0001 | c0001 | t0016 | g0269 | EAS | CHB | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18747 | hp1 | a0001 | c0001 | t0018 | g0193 | EAS | CHB | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18747 | hp2 | a0001 | c0001 | t0006 | g0224 | EAS | CHB | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0237 | AFR | YRI | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18939 | hp1 | a0001 | c0001 | t0004 | g0245 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18941 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18941 | hp2 | a0001 | c0001 | t0016 | g0008 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18942 | hp1 | a0001 | c0001 | t0031 | g0191 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18942 | hp2 | a0001 | c0001 | t0035 | g0097 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18943 | hp1 | a0001 | c0001 | t0004 | g0234 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18943 | hp2 | a0001 | c0001 | t0027 | g0078 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18944 | hp1 | a0001 | c0001 | t0005 | g0171 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18944 | hp2 | a0001 | c0001 | t0018 | g0196 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0146 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18945 | hp2 | a0001 | c0001 | t0004 | g0047 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18946 | hp2 | a0001 | c0001 | t0075 | g0268 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18947 | hp2 | a0001 | c0001 | t0022 | g0188 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18948 | hp1 | a0001 | c0001 | t0018 | g0194 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18949 | hp1 | a0001 | c0001 | t0006 | g0004 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18952 | hp2 | a0001 | c0001 | t0006 | g0004 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18953 | hp2 | a0001 | c0001 | t0010 | g0027 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18956 | hp2 | a0001 | c0001 | t0006 | g0142 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18957 | hp1 | a0001 | c0001 | t0005 | g0182 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18959 | hp1 | a0001 | c0001 | t0022 | g0187 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18962 | hp2 | a0001 | c0001 | t0032 | g0202 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18964 | hp2 | a0001 | c0001 | t0005 | g0181 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18966 | hp1 | a0001 | c0001 | t0010 | g0064 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18968 | hp1 | a0001 | c0001 | t0004 | g0023 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18969 | hp2 | a0001 | c0001 | t0006 | g0004 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18970 | hp2 | a0001 | c0001 | t0006 | g0045 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18973 | hp1 | a0001 | c0001 | t0004 | g0047 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18973 | hp2 | a0001 | c0001 | t0006 | g0004 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18974 | hp1 | a0001 | c0001 | t0045 | g0080 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18974 | hp2 | a0001 | c0001 | t0006 | g0221 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18975 | hp2 | a0001 | c0001 | t0007 | g0190 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18978 | hp1 | a0001 | c0001 | t0007 | g0020 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18978 | hp2 | a0001 | c0001 | t0026 | g0028 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18980 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18980 | hp2 | a0001 | c0001 | t0006 | g0021 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18981 | hp2 | a0001 | c0001 | t0023 | g0163 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18983 | hp1 | a0001 | c0001 | t0007 | g0199 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18983 | hp2 | a0001 | c0001 | t0066 | g0213 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18984 | hp1 | a0001 | c0001 | t0006 | g0214 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18985 | hp1 | a0001 | c0001 | t0016 | g0008 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18987 | hp1 | a0001 | c0001 | t0004 | g0023 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18987 | hp2 | a0001 | c0001 | t0006 | g0296 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18989 | hp1 | a0001 | c0001 | t0006 | g0219 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18989 | hp2 | a0001 | c0001 | t0026 | g0028 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18990 | hp2 | a0001 | c0001 | t0007 | g0020 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18995 | hp2 | a0001 | c0001 | t0024 | g0025 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18997 | hp2 | a0001 | c0001 | t0032 | g0207 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18998 | hp2 | a0001 | c0001 | t0007 | g0036 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19004 | hp2 | a0001 | c0002 | t0003 | g0103 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19005 | hp1 | a0001 | c0001 | t0079 | g0095 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19005 | hp2 | a0001 | c0001 | t0007 | g0204 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19006 | hp1 | a0001 | c0001 | t0053 | g0121 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19006 | hp2 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19007 | hp2 | a0001 | c0001 | t0006 | g0004 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19010 | hp1 | a0001 | c0001 | t0007 | g0020 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19010 | hp2 | a0001 | c0001 | t0052 | g0291 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0098 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19012 | hp2 | a0001 | c0001 | t0006 | g0004 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19030 | hp1 | a0001 | c0001 | t0005 | g0177 | AFR | LWK | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | LWK | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19043 | hp1 | a0001 | c0001 | t0009 | g0157 | AFR | LWK | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19043 | hp2 | a0001 | c0001 | t0062 | g0141 | AFR | LWK | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19054 | hp1 | a0001 | c0001 | t0007 | g0039 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19057 | hp2 | a0001 | c0001 | t0004 | g0023 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19058 | hp1 | a0001 | c0001 | t0021 | g0084 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19060 | hp2 | a0001 | c0001 | t0018 | g0200 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19062 | hp1 | a0001 | c0001 | t0035 | g0096 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19062 | hp2 | a0001 | c0001 | t0007 | g0206 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19063 | hp2 | a0001 | c0001 | t0007 | g0208 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19065 | hp1 | a0001 | c0001 | t0005 | g0034 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19065 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19067 | hp2 | a0001 | c0001 | t0006 | g0045 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19070 | hp1 | a0001 | c0001 | t0011 | g0048 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19070 | hp2 | a0001 | c0001 | t0007 | g0037 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19072 | hp1 | a0001 | c0001 | t0005 | g0172 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19072 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19074 | hp1 | a0001 | c0001 | t0016 | g0008 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19078 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19079 | hp1 | a0001 | c0001 | t0031 | g0198 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19079 | hp2 | a0001 | c0001 | t0006 | g0225 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19080 | hp1 | a0001 | c0001 | t0023 | g0162 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19081 | hp2 | a0001 | c0001 | t0007 | g0195 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19082 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19082 | hp2 | a0001 | c0001 | t0006 | g0021 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19083 | hp1 | a0001 | c0001 | t0078 | g0104 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19083 | hp2 | a0001 | c0001 | t0044 | g0086 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19085 | hp1 | a0001 | c0001 | t0007 | g0192 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19088 | hp1 | a0001 | c0001 | t0016 | g0008 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19240 | hp1 | a0001 | c0001 | t0009 | g0006 | AFR | YRI | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA19240 | hp2 | a0001 | c0001 | t0036 | g0298 | AFR | YRI | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA20129 | hp1 | a0001 | c0001 | t0005 | g0042 | AFR | ASW | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA20129 | hp2 | a0001 | c0001 | t0008 | g0018 | AFR | ASW | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA20752 | hp1 | a0001 | c0001 | t0010 | g0071 | EUR | TSI | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0007 | EUR | TSI | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA20805 | hp1 | a0001 | c0001 | t0039 | g0056 | EUR | TSI | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA20805 | hp2 | a0001 | c0001 | t0005 | g0003 | EUR | TSI | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA20905 | hp1 | a0001 | c0001 | t0005 | g0003 | SAS | GIH | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA20905 | hp2 | a0001 | c0001 | t0006 | g0223 | SAS | GIH | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0229 | AFR | ACB | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02109 | hp2 | a0001 | c0001 | t0056 | g0256 | AFR | ACB | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02486 | hp1 | a0001 | c0001 | t0005 | g0178 | AFR | ACB | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02486 | hp2 | a0001 | c0001 | t0076 | g0284 | AFR | ACB | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02559 | hp1 | a0001 | c0001 | t0015 | g0012 | AFR | ACB | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02559 | hp2 | a0001 | c0001 | t0008 | g0110 | AFR | ACB | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0040 | AFR | MSL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0116 | AFR | MSL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0043 | AFR | USA | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG06807 | hp2 | a0001 | c0001 | t0011 | g0049 | AFR | USA | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA18955 | hp2 | a0001 | c0001 | t0007 | g0197 | EAS | JPT | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA20300 | hp1 | a0001 | c0001 | t0057 | g0262 | AFR | USA | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| NA20300 | hp2 | a0001 | c0001 | t0013 | g0205 | AFR | USA | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0011 | g0264 | REF | REF | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0060 | g0290 | REF | REF | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:3821884
|
C | T | 1 | a0001c0002 | 1 | NA19004.hp2 | synonymous_variant | LOW | c.537G>A | p.Glu179Glu | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/8 | 707/4449 | 537/1017 | 179/338 | chr12 | 3821884 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:3808872
|
G | A | 5 | a0001c0001t0006a0001c0001t0046a0001c0001t0058others(2): Show | 29 | HG00408.hp1 HG00544.hp2 HG02135.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*3251C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 3251 | chr12 | 3808872 | |||||
| chr12:3808998
|
T | G | 1 | a0001c0001t0071 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3125A>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 3125 | chr12 | 3808998 | |||||
| chr12:3809020
|
CT | C | 39 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(36): Show | 203 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(200): Show |
3_prime_UTR_variant | MODIFIER | c.*3102delA | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 3102 | chr12 | 3809020 | |||||
| chr12:3809022
|
T | TTTTTTAT others(7): Show |
8 | a0001c0001t0005a0001c0001t0027a0001c0001t0042others(5): Show | 44 | HG00639.hp2 HG01081.hp1 HG01106.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*3100_*3101insTGTG others(10): Show |
PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 3100 | chr12 | 3809022 | |||||
| chr12:3809134
|
G | T | 5 | a0001c0001t0005a0001c0001t0027a0001c0001t0042others(2): Show | 41 | HG00639.hp2 HG01081.hp1 HG01106.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*2989C>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 2989 | chr12 | 3809134 | |||||
| chr12:3809250
|
T | A | 1 | a0001c0001t0073 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2873A>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 2873 | chr12 | 3809250 | |||||
| chr12:3809309
|
G | A | 61 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(58): Show | 284 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(281): Show |
3_prime_UTR_variant | MODIFIER | c.*2814C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 2814 | chr12 | 3809309 | |||||
| chr12:3809354
|
TAA | T | 5 | a0001c0001t0005a0001c0001t0027a0001c0001t0042others(2): Show | 41 | HG00639.hp2 HG01081.hp1 HG01106.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*2767_*2768delTT | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 2767 | chr12 | 3809354 | |||||
| chr12:3809386
|
A | G | 11 | a0001c0001t0007a0001c0001t0013a0001c0001t0018others(8): Show | 41 | HG01106.hp1 HG01496.hp1 HG01934.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*2737T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 2737 | chr12 | 3809386 | |||||
| chr12:3809556
|
A | AT | 79 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(76): Show | 415 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(412): Show |
3_prime_UTR_variant | MODIFIER | c.*2566_*2567insA | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 2566 | chr12 | 3809556 | |||||
| chr12:3809586
|
G | GT | 2 | a0001c0001t0019a0001c0001t0036 | 6 | HG01346.hp1 HG02280.hp1 HG02717.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2536dupA | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 2536 | chr12 | 3809586 | |||||
| chr12:3809706
|
C | A | 30 | a0001c0001t0003a0001c0001t0005a0001c0001t0006others(27): Show | 154 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(151): Show |
3_prime_UTR_variant | MODIFIER | c.*2417G>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 2417 | chr12 | 3809706 | |||||
| chr12:3809707
|
G | C | 1 | a0001c0001t0050 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2416C>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 2416 | chr12 | 3809707 | |||||
| chr12:3809812
|
T | C | 1 | a0001c0001t0078 | 1 | NA19083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2311A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 2311 | chr12 | 3809812 | |||||
| chr12:3809996
|
A | G | 6 | a0001c0001t0003a0001c0001t0035a0001c0001t0077others(3): Show | 46 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*2127T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 2127 | chr12 | 3809996 | |||||
| chr12:3810037
|
T | C | 1 | a0001c0001t0062 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2086A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 2086 | chr12 | 3810037 | |||||
| chr12:3810080
|
G | A | 1 | a0001c0001t0061 | 1 | HG01069.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2043C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 2043 | chr12 | 3810080 | |||||
| chr12:3810401
|
C | T | 3 | a0001c0001t0033a0001c0001t0064a0001c0001t0065 | 4 | HG02622.hp1 HG02976.hp2 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1722G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 1722 | chr12 | 3810401 | |||||
| chr12:3810418
|
C | T | 1 | a0001c0001t0055 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1705G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 1705 | chr12 | 3810418 | |||||
| chr12:3810503
|
T | C | 5 | a0001c0001t0005a0001c0001t0027a0001c0001t0042others(2): Show | 41 | HG00639.hp2 HG01081.hp1 HG01106.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1620A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 1620 | chr12 | 3810503 | |||||
| chr12:3810514
|
C | T | 1 | a0001c0001t0038 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1609G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 1609 | chr12 | 3810514 | |||||
| chr12:3810598
|
A | G | 1 | a0001c0001t0059 | 1 | HG01934.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1525T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 1525 | chr12 | 3810598 | |||||
| chr12:3810641
|
G | A | 3 | a0001c0001t0003a0001c0001t0035a0001c0002t0003 | 43 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*1482C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 1482 | chr12 | 3810641 | |||||
| chr12:3810642
|
G | A | 2 | a0001c0001t0003a0001c0002t0003 | 41 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1481C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 1481 | chr12 | 3810642 | |||||
| chr12:3810646
|
A | AGAAG | 10 | a0001c0001t0006a0001c0001t0011a0001c0001t0016others(7): Show | 49 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*1473_*1476dupCTTC | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 1476 | chr12 | 3810646 | |||||
| chr12:3810646
|
A | AGAAGGAA others(1): Show |
7 | a0001c0001t0019a0001c0001t0049a0001c0001t0051others(4): Show | 10 | HG01346.hp1 HG01891.hp2 HG02074.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1469_*1476dupCTTC others(4): Show |
PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 1476 | chr12 | 3810646 | |||||
| chr12:3810646
|
A | AGAAGGAA others(5): Show |
5 | a0001c0001t0030a0001c0001t0032a0001c0001t0033others(2): Show | 8 | HG01496.hp1 HG01934.hp1 HG02622.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1465_*1476dupCTTC others(8): Show |
PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 1476 | chr12 | 3810646 | |||||
| chr12:3810646
|
A | AGAAGGAA others(9): Show |
6 | a0001c0001t0007a0001c0001t0013a0001c0001t0022others(3): Show | 30 | HG01106.hp1 HG01975.hp2 HG01981.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1461_*1476dupCTTC others(12): Show |
PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 1476 | chr12 | 3810646 | |||||
| chr12:3810646
|
A | AGAAGGAA others(13): Show |
2 | a0001c0001t0018a0001c0001t0048 | 5 | HG02132.hp2 NA18747.hp1 NA18944.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1457_*1476dupCTTC others(16): Show |
PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 1476 | chr12 | 3810646 | |||||
| chr12:3810646
|
A | AGAAGGAA others(17): Show |
1 | a0001c0001t0031 | 2 | NA18942.hp1 NA19079.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1453_*1476dupCTTC others(20): Show |
PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 1476 | chr12 | 3810646 | |||||
| chr12:3810646
|
A | G | 3 | a0001c0001t0003a0001c0001t0035a0001c0002t0003 | 43 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*1477T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 1477 | chr12 | 3810646 | |||||
| chr12:3810646
|
AGAAG | A | 8 | a0001c0001t0002a0001c0001t0012a0001c0001t0015others(5): Show | 64 | HG00438.hp2 HG00558.hp1 HG00621.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*1473_*1476delCTTC | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 1473 | chr12 | 3810646 | |||||
| chr12:3810646
|
AGAAGGAA others(1): Show |
A | 12 | a0001c0001t0008a0001c0001t0009a0001c0001t0010others(9): Show | 52 | HG00741.hp1 HG01169.hp1 HG01255.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*1469_*1476delCTTC others(4): Show |
PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 1469 | chr12 | 3810646 | |||||
| chr12:3810646
|
AGAAGGAA others(5): Show |
A | 7 | a0001c0001t0005a0001c0001t0027a0001c0001t0038others(4): Show | 43 | HG00408.hp1 HG00639.hp2 HG01081.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*1465_*1476delCTTC others(8): Show |
PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 1465 | chr12 | 3810646 | |||||
| chr12:3810646
|
AGAAGGAA others(9): Show |
A | 4 | a0001c0001t0001a0001c0001t0026a0001c0001t0029others(1): Show | 50 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*1461_*1476delCTTC others(12): Show |
PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 1461 | chr12 | 3810646 | |||||
| chr12:3810646
|
AGAAGGAA others(17): Show |
A | 1 | a0001c0001t0039 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1453_*1476delCTTC others(20): Show |
PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 1453 | chr12 | 3810646 | |||||
| chr12:3810650
|
G | A | 1 | a0001c0001t0079 | 1 | NA19005.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1473C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 1473 | chr12 | 3810650 | |||||
| chr12:3810686
|
A | G | 3 | a0001c0001t0033a0001c0001t0064a0001c0001t0065 | 4 | HG02622.hp1 HG02976.hp2 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1437T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 1437 | chr12 | 3810686 | |||||
| chr12:3810706
|
GAGAGA | G | 5 | a0001c0001t0001a0001c0001t0013a0001c0001t0026others(2): Show | 56 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*1412_*1416delTCTC others(1): Show |
PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 1412 | chr12 | 3810706 | |||||
| chr12:3810710
|
GAAGAGAA others(4): Show |
G | 1 | a0001c0001t0029 | 2 | HG01109.hp1 HG02735.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1402_*1412delTCTC others(7): Show |
PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 1402 | chr12 | 3810710 | |||||
| chr12:3810715
|
G | GA | 14 | a0001c0001t0007a0001c0001t0015a0001c0001t0018others(11): Show | 47 | HG01346.hp1 HG01952.hp2 HG02015.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*1407dupT | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 1407 | chr12 | 3810715 | |||||
| chr12:3810715
|
G | GAAGAGA | 15 | a0001c0001t0005a0001c0001t0006a0001c0001t0009others(12): Show | 87 | HG00408.hp1 HG00639.hp2 HG01081.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*1402_*1407dupTCTC others(2): Show |
PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 1407 | chr12 | 3810715 | |||||
| chr12:3810715
|
G | GAAGAGAA others(5): Show |
2 | a0001c0001t0034a0001c0001t0074 | 3 | HG02027.hp2 HG02622.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1396_*1407dupTCTC others(8): Show |
PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 1407 | chr12 | 3810715 | |||||
| chr12:3810715
|
G | GAAGAGAA others(11): Show |
1 | a0001c0001t0028 | 2 | HG01261.hp2 HG01358.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1390_*1407dupTCTC others(14): Show |
PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 1407 | chr12 | 3810715 | |||||
| chr12:3810715
|
GAAGAGA | G | 6 | a0001c0001t0017a0001c0001t0023a0001c0001t0037others(3): Show | 11 | HG00323.hp1 HG00642.hp1 HG01168.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1402_*1407delTCTC others(2): Show |
PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 1402 | chr12 | 3810715 | |||||
| chr12:3810734
|
AAG | A | 6 | a0001c0001t0003a0001c0001t0035a0001c0001t0077others(3): Show | 46 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*1387_*1388delCT | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 1387 | chr12 | 3810734 | |||||
| chr12:3810747
|
A | T | 1 | a0001c0001t0050 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1376T>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 1376 | chr12 | 3810747 | |||||
| chr12:3810788
|
G | A | 10 | a0001c0001t0009a0001c0001t0017a0001c0001t0023others(7): Show | 26 | HG00323.hp1 HG00642.hp1 HG01168.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1335C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 1335 | chr12 | 3810788 | |||||
| chr12:3810861
|
G | C | 1 | a0001c0001t0072 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1262C>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 1262 | chr12 | 3810861 | |||||
| chr12:3810886
|
G | C | 5 | a0001c0001t0005a0001c0001t0027a0001c0001t0042others(2): Show | 41 | HG00639.hp2 HG01081.hp1 HG01106.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1237C>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 1237 | chr12 | 3810886 | |||||
| chr12:3810947
|
G | A | 1 | a0001c0001t0028 | 2 | HG01261.hp2 HG01358.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1176C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 1176 | chr12 | 3810947 | |||||
| chr12:3811144
|
G | T | 3 | a0001c0001t0022a0001c0001t0048a0001c0001t0049 | 5 | HG02074.hp2 HG02132.hp2 HG02155.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*979C>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 979 | chr12 | 3811144 | |||||
| chr12:3811247
|
G | A | 2 | a0001c0001t0016a0001c0001t0075 | 7 | HG00621.hp1 NA18612.hp2 NA18941.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*876C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 876 | chr12 | 3811247 | |||||
| chr12:3811421
|
A | G | 1 | a0001c0001t0028 | 2 | HG01261.hp2 HG01358.hp1 |
3_prime_UTR_variant | MODIFIER | c.*702T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 702 | chr12 | 3811421 | |||||
| chr12:3811430
|
T | C | 1 | a0001c0001t0076 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*693A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 693 | chr12 | 3811430 | |||||
| chr12:3811494
|
C | A | 1 | a0001c0001t0025 | 2 | HG01255.hp2 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*629G>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 629 | chr12 | 3811494 | |||||
| chr12:3812000
|
CT | C | 6 | a0001c0001t0003a0001c0001t0035a0001c0001t0077others(3): Show | 46 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*122delA | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 122 | chr12 | 3812000 | |||||
| chr12:3812021
|
A | G | 1 | a0001c0001t0047 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*102T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 102 | chr12 | 3812021 | |||||
| chr12:3812077
|
C | T | 1 | a0001c0001t0040 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*46G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 8/8 | 46 | chr12 | 3812077 | |||||
| chr12:3873295
|
A | AT | 8 | a0001c0001t0021a0001c0001t0026a0001c0001t0027others(5): Show | 12 | HG00438.hp1 HG00639.hp2 HG01175.hp1 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-67dupA | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/8 | 67 | chr12 | 3873295 | |||||
| chr12:3873309
|
C | T | 8 | a0001c0001t0010a0001c0001t0012a0001c0001t0020others(5): Show | 26 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(23): Show |
5_prime_UTR_variant | MODIFIER | c.-80G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/8 | 80 | chr12 | 3873309 | |||||
| chr12:3873316
|
C | T | 3 | a0001c0001t0017a0001c0001t0037a0001c0001t0038 | 6 | HG00323.hp1 HG00642.hp1 HG01168.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-87G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/8 | 87 | chr12 | 3873316 | |||||
| chr12:3873320
|
G | A | 2 | a0001c0001t0019a0001c0001t0036 | 6 | HG01346.hp1 HG02280.hp1 HG02717.hp2 others(3): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-91C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/8 | chr12 | 3873320 | ||||||
| chr12:3873370
|
C | T | 1 | a0001c0001t0024 | 2 | HG01433.hp1 NA18995.hp2 |
5_prime_UTR_variant | MODIFIER | c.-141G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/8 | 141 | chr12 | 3873370 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:3812581
|
AGAG | A | 7 | a0001c0001t0011g0168a0001c0001t0014g0118a0001c0001t0014g0165others(4): Show | 7 | HG01192.hp1 HG01358.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.701-145_701-143del others(3): Show |
PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 7/7 | chr12 | 3812581 | ||||||
| chr12:3812622
|
T | C | 1 | a0001c0001t0011g0271 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.701-183A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 7/7 | chr12 | 3812622 | ||||||
| chr12:3812776
|
T | A | 32 | a0001c0001t0007g0020a0001c0001t0007g0036a0001c0001t0007g0037others(29): Show | 41 | HG01106.hp1 HG01496.hp1 HG01934.hp1 others(38): Show |
intron_variant | MODIFIER | c.701-337A>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 7/7 | chr12 | 3812776 | ||||||
| chr12:3812831
|
C | A | 1 | a0001c0001t0006g0225 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.701-392G>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 7/7 | chr12 | 3812831 | ||||||
| chr12:3812948
|
G | GCGTGC | 21 | a0001c0001t0006g0004a0001c0001t0006g0021a0001c0001t0006g0045others(18): Show | 29 | HG00408.hp1 HG00544.hp2 HG02135.hp2 others(26): Show |
intron_variant | MODIFIER | c.701-514_701-510dup others(5): Show |
PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 7/7 | chr12 | 3812948 | ||||||
| chr12:3812976
|
T | C | 3 | a0001c0001t0001g0133a0001c0001t0001g0135a0001c0001t0029g0134 | 3 | HG01109.hp1 HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.701-537A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 7/7 | chr12 | 3812976 | ||||||
| chr12:3812979
|
T | A | 27 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(24): Show | 47 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.701-540A>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 7/7 | chr12 | 3812979 | ||||||
| chr12:3813073
|
G | A | 1 | a0001c0001t0063g0148 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.701-634C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 7/7 | chr12 | 3813073 | ||||||
| chr12:3813100
|
C | T | 79 | a0001c0001t0003g0001a0001c0001t0003g0013a0001c0001t0003g0014others(76): Show | 113 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.701-661G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 7/7 | chr12 | 3813100 | ||||||
| chr12:3813184
|
A | G | 1 | a0001c0001t0025g0068 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.701-745T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 7/7 | chr12 | 3813184 | ||||||
| chr12:3813263
|
T | C | 28 | a0001c0001t0003g0001a0001c0001t0003g0013a0001c0001t0003g0014others(25): Show | 46 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.700+774A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 7/7 | chr12 | 3813263 | ||||||
| chr12:3813314
|
A | G | 1 | a0001c0001t0028g0035 | 2 | HG01261.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.700+723T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 7/7 | chr12 | 3813314 | ||||||
| chr12:3813669
|
C | T | 79 | a0001c0001t0003g0001a0001c0001t0003g0013a0001c0001t0003g0014others(76): Show | 113 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.700+368G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 7/7 | chr12 | 3813669 | ||||||
| chr12:3813895
|
G | A | 15 | a0001c0001t0009g0006a0001c0001t0009g0032a0001c0001t0009g0153others(12): Show | 23 | HG00323.hp1 HG00642.hp1 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.700+142C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 7/7 | chr12 | 3813895 | ||||||
| chr12:3814332
|
G | C | 21 | a0001c0001t0006g0004a0001c0001t0006g0021a0001c0001t0006g0045others(18): Show | 29 | HG00408.hp1 HG00544.hp2 HG02135.hp2 others(26): Show |
intron_variant | MODIFIER | c.549-144C>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3814332 | ||||||
| chr12:3814406
|
A | G | 21 | a0001c0001t0006g0004a0001c0001t0006g0021a0001c0001t0006g0045others(18): Show | 29 | HG00408.hp1 HG00544.hp2 HG02135.hp2 others(26): Show |
intron_variant | MODIFIER | c.549-218T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3814406 | ||||||
| chr12:3814532
|
C | T | 22 | a0001c0001t0005g0003a0001c0001t0005g0033a0001c0001t0005g0034others(19): Show | 31 | HG00639.hp2 HG01081.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.549-344G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3814532 | ||||||
| chr12:3814607
|
A | G | 1 | a0001c0001t0010g0073 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.549-419T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3814607 | ||||||
| chr12:3814677
|
A | G | 1 | a0001c0001t0003g0100 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.549-489T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3814677 | ||||||
| chr12:3814681
|
T | C | 1 | a0001c0001t0002g0288 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.549-493A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3814681 | ||||||
| chr12:3814696
|
A | T | 21 | a0001c0001t0006g0004a0001c0001t0006g0021a0001c0001t0006g0045others(18): Show | 29 | HG00408.hp1 HG00544.hp2 HG02135.hp2 others(26): Show |
intron_variant | MODIFIER | c.549-508T>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3814696 | ||||||
| chr12:3814791
|
A | AAT | 197 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(194): Show | 285 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(282): Show |
intron_variant | MODIFIER | c.549-605_549-604dup others(2): Show |
PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3814791 | ||||||
| chr12:3815192
|
A | C | 15 | a0001c0001t0009g0006a0001c0001t0009g0032a0001c0001t0009g0153others(12): Show | 23 | HG00323.hp1 HG00642.hp1 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.549-1004T>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3815192 | ||||||
| chr12:3815201
|
C | G | 78 | a0001c0001t0002g0273a0001c0001t0003g0001a0001c0001t0003g0013others(75): Show | 115 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.549-1013G>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3815201 | ||||||
| chr12:3815932
|
T | C | 92 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(89): Show | 133 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(130): Show |
intron_variant | MODIFIER | c.549-1744A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3815932 | ||||||
| chr12:3816004
|
T | C | 1 | a0001c0001t0063g0148 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.549-1816A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3816004 | ||||||
| chr12:3816060
|
C | T | 92 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(89): Show | 133 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(130): Show |
intron_variant | MODIFIER | c.549-1872G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3816060 | ||||||
| chr12:3816186
|
G | A | 1 | a0001c0001t0006g0215 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.549-1998C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3816186 | ||||||
| chr12:3816204
|
TA | T | 22 | a0001c0001t0005g0003a0001c0001t0005g0033a0001c0001t0005g0034others(19): Show | 31 | HG00639.hp2 HG01081.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.549-2017delT | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3816204 | ||||||
| chr12:3816260
|
C | T | 18 | a0001c0001t0009g0006a0001c0001t0009g0032a0001c0001t0009g0153others(15): Show | 26 | HG00323.hp1 HG00642.hp1 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.549-2072G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3816260 | ||||||
| chr12:3816395
|
C | A | 1 | a0001c0001t0002g0293 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.549-2207G>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3816395 | ||||||
| chr12:3816419
|
G | A | 10 | a0001c0001t0009g0006a0001c0001t0009g0158a0001c0001t0009g0159others(7): Show | 17 | HG00323.hp1 HG00642.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.549-2231C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3816419 | ||||||
| chr12:3816468
|
A | G | 1 | a0001c0001t0002g0138 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.549-2280T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3816468 | ||||||
| chr12:3816834
|
G | A | 2 | a0001c0001t0034g0136a0001c0001t0034g0137 | 2 | HG02622.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.549-2646C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3816834 | ||||||
| chr12:3816943
|
G | C | 1 | a0001c0001t0001g0133 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.549-2755C>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3816943 | ||||||
| chr12:3816974
|
G | A | 1 | a0001c0001t0002g0280 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.549-2786C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3816974 | ||||||
| chr12:3816999
|
A | G | 20 | a0001c0001t0009g0006a0001c0001t0009g0032a0001c0001t0009g0153others(17): Show | 29 | HG00323.hp1 HG00642.hp1 HG01168.hp2 others(26): Show |
intron_variant | MODIFIER | c.549-2811T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3816999 | ||||||
| chr12:3817117
|
G | A | 1 | a0001c0001t0069g0147 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.549-2929C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3817117 | ||||||
| chr12:3817135
|
G | A | 92 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(89): Show | 133 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(130): Show |
intron_variant | MODIFIER | c.549-2947C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3817135 | ||||||
| chr12:3817146
|
G | A | 5 | a0001c0001t0019g0053a0001c0001t0019g0297a0001c0001t0019g0299others(2): Show | 6 | HG01346.hp1 HG02280.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.549-2958C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3817146 | ||||||
| chr12:3817190
|
C | CA | 163 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(160): Show | 237 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.549-3003dupT | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3817190 | ||||||
| chr12:3817190
|
C | CAA | 32 | a0001c0001t0005g0003a0001c0001t0005g0033a0001c0001t0005g0034others(29): Show | 46 | HG00639.hp2 HG01081.hp1 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.549-3004_549-3003d others(4): Show |
PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3817190 | ||||||
| chr12:3817228
|
A | G | 1 | a0001c0001t0010g0065 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.549-3040T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3817228 | ||||||
| chr12:3817278
|
T | C | 5 | a0001c0001t0015g0012a0001c0001t0015g0030a0001c0001t0033g0044others(2): Show | 10 | HG01952.hp2 HG02258.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.549-3090A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3817278 | ||||||
| chr12:3817312
|
G | A | 1 | a0001c0001t0071g0230 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.549-3124C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3817312 | ||||||
| chr12:3817451
|
A | G | 5 | a0001c0001t0019g0053a0001c0001t0019g0297a0001c0001t0019g0299others(2): Show | 6 | HG01346.hp1 HG02280.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.549-3263T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3817451 | ||||||
| chr12:3817460
|
A | G | 1 | a0001c0001t0019g0053 | 2 | HG01346.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.549-3272T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3817460 | ||||||
| chr12:3817574
|
C | T | 3 | a0001c0001t0033g0044a0001c0001t0064g0211a0001c0001t0065g0212 | 4 | HG02622.hp1 HG02976.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.549-3386G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3817574 | ||||||
| chr12:3817634
|
C | T | 92 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(89): Show | 133 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(130): Show |
intron_variant | MODIFIER | c.549-3446G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3817634 | ||||||
| chr12:3817707
|
G | A | 29 | a0001c0001t0005g0003a0001c0001t0005g0033a0001c0001t0005g0034others(26): Show | 41 | HG00639.hp2 HG01081.hp1 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.549-3519C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3817707 | ||||||
| chr12:3817818
|
T | G | 4 | a0001c0001t0019g0297a0001c0001t0019g0299a0001c0001t0036g0298others(1): Show | 4 | HG02280.hp1 HG03130.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.549-3630A>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3817818 | ||||||
| chr12:3817873
|
G | C | 3 | a0001c0001t0033g0044a0001c0001t0064g0211a0001c0001t0065g0212 | 4 | HG02622.hp1 HG02976.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.549-3685C>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3817873 | ||||||
| chr12:3817959
|
T | G | 1 | a0001c0001t0005g0180 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.549-3771A>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3817959 | ||||||
| chr12:3818142
|
G | T | 2 | a0001c0001t0005g0177a0001c0001t0005g0178 | 2 | HG02486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.548+3731C>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3818142 | ||||||
| chr12:3818445
|
G | A | 1 | a0001c0001t0025g0068 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.548+3428C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3818445 | ||||||
| chr12:3818524
|
A | G | 1 | a0001c0001t0004g0242 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.548+3349T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3818524 | ||||||
| chr12:3818562
|
C | G | 1 | a0001c0001t0038g0055 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.548+3311G>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3818562 | ||||||
| chr12:3818592
|
T | C | 1 | a0001c0001t0002g0274 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.548+3281A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3818592 | ||||||
| chr12:3819008
|
A | T | 28 | a0001c0001t0003g0001a0001c0001t0003g0013a0001c0001t0003g0014others(25): Show | 46 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.548+2865T>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3819008 | ||||||
| chr12:3819046
|
C | G | 270 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(267): Show | 376 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(373): Show |
intron_variant | MODIFIER | c.548+2827G>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3819046 | ||||||
| chr12:3819201
|
C | T | 2 | a0001c0001t0069g0147a0001c0001t0070g0139 | 2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.548+2672G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3819201 | ||||||
| chr12:3819304
|
C | T | 92 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(89): Show | 133 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(130): Show |
intron_variant | MODIFIER | c.548+2569G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3819304 | ||||||
| chr12:3819459
|
T | C | 5 | a0001c0001t0019g0053a0001c0001t0019g0297a0001c0001t0019g0299others(2): Show | 6 | HG01346.hp1 HG02280.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.548+2414A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3819459 | ||||||
| chr12:3819516
|
A | T | 1 | a0001c0001t0004g0237 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.548+2357T>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3819516 | ||||||
| chr12:3819716
|
C | A | 1 | a0001c0001t0028g0035 | 2 | HG01261.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.548+2157G>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3819716 | ||||||
| chr12:3819736
|
G | T | 1 | a0001c0001t0002g0292 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.548+2137C>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3819736 | ||||||
| chr12:3819867
|
C | A | 18 | a0001c0001t0009g0006a0001c0001t0009g0032a0001c0001t0009g0153others(15): Show | 26 | HG00323.hp1 HG00642.hp1 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.548+2006G>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3819867 | ||||||
| chr12:3820194
|
T | G | 1 | a0001c0001t0004g0245 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.548+1679A>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3820194 | ||||||
| chr12:3820275
|
T | G | 1 | a0001c0001t0003g0106 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.548+1598A>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3820275 | ||||||
| chr12:3820310
|
G | C | 1 | a0001c0001t0009g0159 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.548+1563C>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3820310 | ||||||
| chr12:3820328
|
C | G | 1 | a0001c0001t0010g0075 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.548+1545G>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3820328 | ||||||
| chr12:3820839
|
T | C | 1 | a0001c0001t0009g0155 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.548+1034A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3820839 | ||||||
| chr12:3821107
|
G | A | 23 | a0001c0001t0011g0048a0001c0001t0011g0049a0001c0001t0011g0168others(20): Show | 29 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(26): Show |
intron_variant | MODIFIER | c.548+766C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3821107 | ||||||
| chr12:3821376
|
T | C | 1 | a0001c0001t0063g0148 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.548+497A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3821376 | ||||||
| chr12:3821397
|
C | T | 1 | a0001c0001t0070g0139 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.548+476G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3821397 | ||||||
| chr12:3821408
|
T | C | 28 | a0001c0001t0003g0001a0001c0001t0003g0013a0001c0001t0003g0014others(25): Show | 46 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.548+465A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3821408 | ||||||
| chr12:3821625
|
T | C | 1 | a0001c0001t0002g0275 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.548+248A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3821625 | ||||||
| chr12:3821749
|
T | C | 1 | a0001c0001t0014g0183 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.548+124A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3821749 | ||||||
| chr12:3822365
|
G | A | 1 | a0001c0001t0028g0035 | 2 | HG01261.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.345-208C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3822365 | ||||||
| chr12:3822371
|
A | G | 95 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(92): Show | 140 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(137): Show |
intron_variant | MODIFIER | c.345-214T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3822371 | ||||||
| chr12:3822381
|
G | A | 3 | a0001c0001t0001g0133a0001c0001t0001g0135a0001c0001t0029g0134 | 3 | HG01109.hp1 HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.345-224C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3822381 | ||||||
| chr12:3822386
|
CAGG | C | 4 | a0001c0001t0005g0040a0001c0001t0005g0041a0001c0001t0005g0042others(1): Show | 7 | HG01884.hp2 HG02257.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.345-232_345-230del others(3): Show |
PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3822386 | ||||||
| chr12:3822442
|
CA | C | 97 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(94): Show | 142 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(139): Show |
intron_variant | MODIFIER | c.345-286delT | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3822442 | ||||||
| chr12:3822456
|
A | G | 92 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(89): Show | 135 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(132): Show |
intron_variant | MODIFIER | c.345-299T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3822456 | ||||||
| chr12:3822462
|
G | T | 9 | a0001c0001t0002g0116a0001c0001t0008g0016a0001c0001t0008g0018others(6): Show | 13 | HG01169.hp1 HG02055.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.345-305C>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3822462 | ||||||
| chr12:3822464
|
G | T | 92 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(89): Show | 135 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(132): Show |
intron_variant | MODIFIER | c.345-307C>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3822464 | ||||||
| chr12:3822515
|
C | T | 28 | a0001c0001t0003g0001a0001c0001t0003g0013a0001c0001t0003g0014others(25): Show | 46 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.345-358G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3822515 | ||||||
| chr12:3822516
|
G | A | 2 | a0001c0001t0069g0147a0001c0001t0070g0139 | 2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.345-359C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3822516 | ||||||
| chr12:3822553
|
T | C | 2 | a0001c0001t0005g0171a0001c0001t0054g0263 | 2 | HG02523.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.345-396A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3822553 | ||||||
| chr12:3822578
|
G | A | 1 | a0001c0001t0013g0203 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.345-421C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3822578 | ||||||
| chr12:3822585
|
C | T | 5 | a0001c0001t0019g0053a0001c0001t0019g0297a0001c0001t0019g0299others(2): Show | 6 | HG01346.hp1 HG02280.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.345-428G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3822585 | ||||||
| chr12:3822598
|
C | CA | 13 | a0001c0001t0002g0248a0001c0001t0002g0276a0001c0001t0002g0278others(10): Show | 14 | HG01981.hp2 HG02055.hp2 HG02523.hp2 others(11): Show |
intron_variant | MODIFIER | c.345-442dupT | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3822598 | ||||||
| chr12:3822598
|
CA | C | 115 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(112): Show | 165 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.345-442delT | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3822598 | ||||||
| chr12:3822631
|
A | G | 1 | a0001c0001t0002g0246 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.345-474T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3822631 | ||||||
| chr12:3822732
|
G | GT | 26 | a0001c0001t0003g0001a0001c0001t0003g0013a0001c0001t0003g0014others(23): Show | 44 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.345-576dupA | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3822732 | ||||||
| chr12:3822773
|
A | G | 31 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(28): Show | 51 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.345-616T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3822773 | ||||||
| chr12:3822884
|
T | C | 1 | a0001c0001t0009g0159 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.345-727A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3822884 | ||||||
| chr12:3822900
|
T | A | 174 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(171): Show | 253 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(250): Show |
intron_variant | MODIFIER | c.345-743A>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3822900 | ||||||
| chr12:3822959
|
C | G | 1 | a0001c0001t0062g0141 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.345-802G>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3822959 | ||||||
| chr12:3823031
|
T | C | 2 | a0001c0001t0009g0153a0001c0001t0068g0156 | 2 | HG02451.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.345-874A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3823031 | ||||||
| chr12:3823173
|
T | C | 17 | a0001c0001t0002g0273a0001c0001t0011g0048a0001c0001t0011g0049others(14): Show | 23 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(20): Show |
intron_variant | MODIFIER | c.345-1016A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3823173 | ||||||
| chr12:3823195
|
G | C | 95 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(92): Show | 140 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(137): Show |
intron_variant | MODIFIER | c.345-1038C>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3823195 | ||||||
| chr12:3823424
|
G | A | 1 | a0001c0001t0050g0140 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.345-1267C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3823424 | ||||||
| chr12:3823448
|
A | G | 2 | a0001c0001t0002g0022a0001c0001t0004g0232 | 4 | HG00738.hp2 HG01074.hp1 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-1291T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3823448 | ||||||
| chr12:3823461
|
C | T | 172 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(169): Show | 247 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(244): Show |
intron_variant | MODIFIER | c.345-1304G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3823461 | ||||||
| chr12:3823482
|
C | T | 1 | a0001c0001t0003g0101 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.345-1325G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3823482 | ||||||
| chr12:3823499
|
T | C | 1 | a0001c0001t0065g0212 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.345-1342A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3823499 | ||||||
| chr12:3823512
|
G | GT | 29 | a0001c0001t0005g0003a0001c0001t0005g0033a0001c0001t0005g0034others(26): Show | 41 | HG00639.hp2 HG01081.hp1 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.345-1356dupA | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3823512 | ||||||
| chr12:3823536
|
T | C | 5 | a0001c0001t0019g0053a0001c0001t0019g0297a0001c0001t0019g0299others(2): Show | 6 | HG01346.hp1 HG02280.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.345-1379A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3823536 | ||||||
| chr12:3823554
|
C | T | 93 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(90): Show | 134 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(131): Show |
intron_variant | MODIFIER | c.345-1397G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3823554 | ||||||
| chr12:3823714
|
G | A | 2 | a0001c0001t0006g0221a0001c0001t0058g0220 | 2 | HG00544.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.345-1557C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3823714 | ||||||
| chr12:3823826
|
G | T | 1 | a0001c0001t0023g0163 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.345-1669C>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3823826 | ||||||
| chr12:3823859
|
T | C | 1 | a0001c0001t0005g0175 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.345-1702A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3823859 | ||||||
| chr12:3823860
|
G | A | 1 | a0001c0001t0050g0140 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.345-1703C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3823860 | ||||||
| chr12:3823915
|
C | CA | 13 | a0001c0001t0002g0273a0001c0001t0002g0293a0001c0001t0003g0106others(10): Show | 19 | HG00408.hp1 HG01346.hp2 HG01934.hp2 others(16): Show |
intron_variant | MODIFIER | c.345-1759dupT | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3823915 | ||||||
| chr12:3823915
|
CA | C | 31 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(28): Show | 40 | HG00639.hp2 HG01081.hp1 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.345-1759delT | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3823915 | ||||||
| chr12:3824178
|
T | C | 1 | a0001c0001t0063g0148 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.344+1980A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3824178 | ||||||
| chr12:3824659
|
T | C | 2 | a0001c0001t0001g0122a0001c0001t0001g0132 | 2 | HG00609.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.344+1499A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3824659 | ||||||
| chr12:3824750
|
C | T | 28 | a0001c0001t0003g0001a0001c0001t0003g0013a0001c0001t0003g0014others(25): Show | 46 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.344+1408G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3824750 | ||||||
| chr12:3824851
|
C | A | 1 | a0001c0001t0004g0243 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.344+1307G>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3824851 | ||||||
| chr12:3824871
|
G | A | 5 | a0001c0001t0019g0053a0001c0001t0019g0297a0001c0001t0019g0299others(2): Show | 6 | HG01346.hp1 HG02280.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.344+1287C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3824871 | ||||||
| chr12:3824946
|
A | G | 6 | a0001c0001t0019g0053a0001c0001t0019g0297a0001c0001t0019g0299others(3): Show | 7 | HG01346.hp1 HG02055.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.344+1212T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3824946 | ||||||
| chr12:3825109
|
C | CT | 33 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(30): Show | 57 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.344+1048dupA | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3825109 | ||||||
| chr12:3825133
|
T | A | 2 | a0001c0001t0004g0160a0001c0001t0004g0244 | 2 | HG01071.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.344+1025A>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3825133 | ||||||
| chr12:3825481
|
C | T | 6 | a0001c0001t0019g0053a0001c0001t0019g0297a0001c0001t0019g0299others(3): Show | 7 | HG01346.hp1 HG02055.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.344+677G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3825481 | ||||||
| chr12:3825536
|
T | C | 1 | a0001c0001t0009g0159 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.344+622A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3825536 | ||||||
| chr12:3825574
|
C | T | 2 | a0001c0001t0008g0108a0001c0001t0008g0110 | 2 | HG02559.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.344+584G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3825574 | ||||||
| chr12:3825654
|
A | C | 32 | a0001c0001t0007g0020a0001c0001t0007g0036a0001c0001t0007g0037others(29): Show | 41 | HG01106.hp1 HG01496.hp1 HG01934.hp1 others(38): Show |
intron_variant | MODIFIER | c.344+504T>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3825654 | ||||||
| chr12:3825812
|
C | T | 28 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(25): Show | 48 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.344+346G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3825812 | ||||||
| chr12:3825855
|
T | C | 1 | a0001c0001t0001g0119 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.344+303A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3825855 | ||||||
| chr12:3825930
|
G | A | 5 | a0001c0001t0019g0053a0001c0001t0019g0297a0001c0001t0019g0299others(2): Show | 6 | HG01346.hp1 HG02280.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.344+228C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3825930 | ||||||
| chr12:3825951
|
C | T | 1 | a0001c0001t0063g0148 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.344+207G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3825951 | ||||||
| chr12:3825968
|
ATCAGGCC others(3): Show |
A | 1 | a0001c0001t0009g0157 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.344+180_344+189del others(10): Show |
PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3825968 | ||||||
| chr12:3825983
|
C | G | 1 | a0001c0001t0009g0157 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.344+175G>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3825983 | ||||||
| chr12:3826123
|
A | C | 3 | a0001c0001t0006g0226a0001c0001t0011g0265a0001c0001t0028g0035 | 4 | HG00423.hp2 HG01261.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.344+35T>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 4/7 | chr12 | 3826123 | ||||||
| chr12:3826290
|
G | T | 11 | a0001c0001t0002g0116a0001c0001t0008g0016a0001c0001t0008g0018others(8): Show | 15 | HG01169.hp1 HG02055.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.269-57C>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 3/7 | chr12 | 3826290 | ||||||
| chr12:3826315
|
C | T | 2 | a0001c0001t0015g0012a0001c0001t0015g0030 | 6 | HG01952.hp2 HG02258.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.269-82G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 3/7 | chr12 | 3826315 | ||||||
| chr12:3826383
|
A | G | 2 | a0001c0001t0034g0136a0001c0001t0034g0137 | 2 | HG02622.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.269-150T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 3/7 | chr12 | 3826383 | ||||||
| chr12:3826391
|
A | G | 1 | a0001c0001t0010g0071 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.269-158T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 3/7 | chr12 | 3826391 | ||||||
| chr12:3826449
|
T | A | 1 | a0001c0001t0020g0069 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.269-216A>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 3/7 | chr12 | 3826449 | ||||||
| chr12:3826575
|
G | A | 1 | a0001c0001t0028g0035 | 2 | HG01261.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.269-342C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 3/7 | chr12 | 3826575 | ||||||
| chr12:3826923
|
T | C | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | NA19067.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.269-690A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 3/7 | chr12 | 3826923 | ||||||
| chr12:3826963
|
A | T | 9 | a0001c0001t0002g0116a0001c0001t0008g0016a0001c0001t0008g0018others(6): Show | 13 | HG01169.hp1 HG02055.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.269-730T>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 3/7 | chr12 | 3826963 | ||||||
| chr12:3827012
|
T | C | 1 | a0001c0001t0002g0043 | 2 | HG02970.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.269-779A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 3/7 | chr12 | 3827012 | ||||||
| chr12:3827028
|
T | A | 30 | a0001c0001t0005g0003a0001c0001t0005g0033a0001c0001t0005g0034others(27): Show | 42 | HG00639.hp2 HG01081.hp1 HG01106.hp2 others(39): Show |
intron_variant | MODIFIER | c.269-795A>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 3/7 | chr12 | 3827028 | ||||||
| chr12:3827094
|
G | C | 21 | a0001c0001t0006g0004a0001c0001t0006g0021a0001c0001t0006g0045others(18): Show | 29 | HG00408.hp1 HG00544.hp2 HG02135.hp2 others(26): Show |
intron_variant | MODIFIER | c.269-861C>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 3/7 | chr12 | 3827094 | ||||||
| chr12:3827251
|
C | T | 1 | a0001c0001t0003g0094 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.269-1018G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 3/7 | chr12 | 3827251 | ||||||
| chr12:3827288
|
T | C | 2 | a0001c0001t0034g0136a0001c0001t0034g0137 | 2 | HG02622.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.269-1055A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 3/7 | chr12 | 3827288 | ||||||
| chr12:3827321
|
T | C | 6 | a0001c0001t0012g0026a0001c0001t0012g0057a0001c0001t0012g0061others(3): Show | 7 | HG00735.hp2 HG00738.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.269-1088A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 3/7 | chr12 | 3827321 | ||||||
| chr12:3827370
|
T | C | 84 | a0001c0001t0002g0273a0001c0001t0003g0001a0001c0001t0003g0013others(81): Show | 123 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.269-1137A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 3/7 | chr12 | 3827370 | ||||||
| chr12:3827466
|
T | G | 23 | a0001c0001t0002g0273a0001c0001t0011g0048a0001c0001t0011g0049others(20): Show | 29 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(26): Show |
intron_variant | MODIFIER | c.269-1233A>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 3/7 | chr12 | 3827466 | ||||||
| chr12:3827628
|
C | A | 1 | a0001c0001t0008g0279 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.268+1282G>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 3/7 | chr12 | 3827628 | ||||||
| chr12:3827775
|
T | G | 84 | a0001c0001t0002g0273a0001c0001t0003g0001a0001c0001t0003g0013others(81): Show | 123 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.268+1135A>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 3/7 | chr12 | 3827775 | ||||||
| chr12:3827794
|
G | A | 32 | a0001c0001t0007g0020a0001c0001t0007g0036a0001c0001t0007g0037others(29): Show | 41 | HG01106.hp1 HG01496.hp1 HG01934.hp1 others(38): Show |
intron_variant | MODIFIER | c.268+1116C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 3/7 | chr12 | 3827794 | ||||||
| chr12:3827891
|
T | C | 1 | a0001c0001t0052g0291 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.268+1019A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 3/7 | chr12 | 3827891 | ||||||
| chr12:3828087
|
T | C | 1 | a0001c0001t0023g0163 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.268+823A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 3/7 | chr12 | 3828087 | ||||||
| chr12:3828132
|
C | T | 21 | a0001c0001t0006g0004a0001c0001t0006g0021a0001c0001t0006g0045others(18): Show | 29 | HG00408.hp1 HG00544.hp2 HG02135.hp2 others(26): Show |
intron_variant | MODIFIER | c.268+778G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 3/7 | chr12 | 3828132 | ||||||
| chr12:3828144
|
T | C | 1 | a0001c0001t0005g0175 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.268+766A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 3/7 | chr12 | 3828144 | ||||||
| chr12:3828384
|
T | C | 1 | a0001c0001t0004g0237 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.268+526A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 3/7 | chr12 | 3828384 | ||||||
| chr12:3828497
|
G | A | 93 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(90): Show | 134 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(131): Show |
intron_variant | MODIFIER | c.268+413C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 3/7 | chr12 | 3828497 | ||||||
| chr12:3828504
|
T | C | 1 | a0001c0001t0070g0139 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.268+406A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 3/7 | chr12 | 3828504 | ||||||
| chr12:3828544
|
C | CA | 19 | a0001c0001t0002g0273a0001c0001t0002g0276a0001c0001t0002g0278others(16): Show | 25 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(22): Show |
intron_variant | MODIFIER | c.268+365dupT | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 3/7 | chr12 | 3828544 | ||||||
| chr12:3828544
|
C | CAA | 8 | a0001c0001t0011g0168a0001c0001t0014g0165a0001c0001t0014g0166others(5): Show | 8 | HG01192.hp1 HG01358.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.268+364_268+365dup others(2): Show |
PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 3/7 | chr12 | 3828544 | ||||||
| chr12:3828544
|
CA | C | 89 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(86): Show | 130 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(127): Show |
intron_variant | MODIFIER | c.268+365delT | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 3/7 | chr12 | 3828544 | ||||||
| chr12:3828630
|
C | T | 5 | a0001c0001t0007g0199a0001c0001t0022g0187a0001c0001t0022g0188others(2): Show | 5 | NA18942.hp1 NA18947.hp2 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.268+280G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 3/7 | chr12 | 3828630 | ||||||
| chr12:3828697
|
A | G | 1 | a0001c0001t0009g0032 | 2 | HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.268+213T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 3/7 | chr12 | 3828697 | ||||||
| chr12:3828759
|
A | T | 9 | a0001c0001t0002g0116a0001c0001t0008g0016a0001c0001t0008g0018others(6): Show | 13 | HG01169.hp1 HG02055.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.268+151T>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 3/7 | chr12 | 3828759 | ||||||
| chr12:3829129
|
C | T | 1 | a0001c0001t0009g0032 | 2 | HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.148-99G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 2/7 | chr12 | 3829129 | ||||||
| chr12:3829130
|
G | A | 1 | a0001c0001t0004g0047 | 2 | NA18945.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.148-100C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 2/7 | chr12 | 3829130 | ||||||
| chr12:3829200
|
G | A | 28 | a0001c0001t0003g0001a0001c0001t0003g0013a0001c0001t0003g0014others(25): Show | 46 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.148-170C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 2/7 | chr12 | 3829200 | ||||||
| chr12:3829231
|
C | T | 1 | a0001c0001t0020g0062 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.148-201G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 2/7 | chr12 | 3829231 | ||||||
| chr12:3829361
|
T | C | 5 | a0001c0001t0015g0012a0001c0001t0015g0030a0001c0001t0033g0044others(2): Show | 10 | HG01952.hp2 HG02258.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.148-331A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 2/7 | chr12 | 3829361 | ||||||
| chr12:3829550
|
C | A | 2 | a0001c0001t0002g0289a0001c0001t0076g0284 | 2 | HG01175.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.147+340G>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 2/7 | chr12 | 3829550 | ||||||
| chr12:3829774
|
T | C | 5 | a0001c0001t0002g0050a0001c0001t0002g0274a0001c0001t0002g0292others(2): Show | 7 | HG01433.hp1 NA18952.hp1 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.147+116A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 2/7 | chr12 | 3829774 | ||||||
| chr12:3830162
|
A | G | 1 | a0001c0001t0059g0241 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.19-144T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3830162 | ||||||
| chr12:3830221
|
A | G | 2 | a0001c0001t0022g0185a0001c0001t0049g0186 | 2 | HG02074.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.19-203T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3830221 | ||||||
| chr12:3830379
|
G | A | 3 | a0001c0001t0004g0251a0001c0001t0021g0083a0001c0001t0061g0235 | 3 | HG01069.hp2 HG01175.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.19-361C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3830379 | ||||||
| chr12:3830392
|
A | T | 3 | a0001c0001t0033g0044a0001c0001t0064g0211a0001c0001t0065g0212 | 4 | HG02622.hp1 HG02976.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-374T>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3830392 | ||||||
| chr12:3830476
|
C | T | 1 | a0001c0001t0002g0286 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.19-458G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3830476 | ||||||
| chr12:3830533
|
C | T | 93 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(90): Show | 134 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(131): Show |
intron_variant | MODIFIER | c.19-515G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3830533 | ||||||
| chr12:3830602
|
A | G | 29 | a0001c0001t0005g0003a0001c0001t0005g0033a0001c0001t0005g0034others(26): Show | 41 | HG00639.hp2 HG01081.hp1 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.19-584T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3830602 | ||||||
| chr12:3830806
|
A | G | 179 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(176): Show | 259 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(256): Show |
intron_variant | MODIFIER | c.19-788T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3830806 | ||||||
| chr12:3831245
|
A | ATC | 2 | a0001c0001t0015g0012a0001c0001t0015g0030 | 6 | HG01952.hp2 HG02258.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.19-1229_19-1228dup others(2): Show |
PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3831245 | ||||||
| chr12:3831258
|
T | C | 1 | a0001c0001t0005g0171 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.19-1240A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3831258 | ||||||
| chr12:3831280
|
TA | T | 32 | a0001c0001t0007g0020a0001c0001t0007g0036a0001c0001t0007g0037others(29): Show | 41 | HG01106.hp1 HG01496.hp1 HG01934.hp1 others(38): Show |
intron_variant | MODIFIER | c.19-1263delT | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3831280 | ||||||
| chr12:3831304
|
T | C | 1 | a0001c0001t0016g0269 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.19-1286A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3831304 | ||||||
| chr12:3831329
|
A | C | 1 | a0001c0001t0003g0090 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.19-1311T>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3831329 | ||||||
| chr12:3831467
|
A | T | 93 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(90): Show | 134 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(131): Show |
intron_variant | MODIFIER | c.19-1449T>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3831467 | ||||||
| chr12:3831513
|
G | A | 1 | a0001c0001t0070g0139 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.19-1495C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3831513 | ||||||
| chr12:3831539
|
T | C | 1 | a0001c0001t0010g0064 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.19-1521A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3831539 | ||||||
| chr12:3831573
|
C | T | 1 | a0001c0001t0007g0197 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.19-1555G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3831573 | ||||||
| chr12:3831636
|
T | A | 2 | a0001c0001t0005g0177a0001c0001t0005g0178 | 2 | HG02486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.19-1618A>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3831636 | ||||||
| chr12:3831863
|
T | A | 3 | a0001c0001t0069g0147a0001c0001t0070g0139a0001c0001t0071g0230 | 3 | HG02615.hp2 HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.19-1845A>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3831863 | ||||||
| chr12:3831875
|
T | C | 1 | a0001c0001t0025g0070 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.19-1857A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3831875 | ||||||
| chr12:3831917
|
A | C | 1 | a0001c0001t0014g0267 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.19-1899T>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3831917 | ||||||
| chr12:3831923
|
G | A | 1 | a0001c0001t0004g0245 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.19-1905C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3831923 | ||||||
| chr12:3832045
|
T | C | 32 | a0001c0001t0007g0020a0001c0001t0007g0036a0001c0001t0007g0037others(29): Show | 41 | HG01106.hp1 HG01496.hp1 HG01934.hp1 others(38): Show |
intron_variant | MODIFIER | c.19-2027A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3832045 | ||||||
| chr12:3832100
|
A | G | 95 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(92): Show | 140 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(137): Show |
intron_variant | MODIFIER | c.19-2082T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3832100 | ||||||
| chr12:3832123
|
C | T | 9 | a0001c0001t0002g0116a0001c0001t0008g0016a0001c0001t0008g0018others(6): Show | 13 | HG01169.hp1 HG02055.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.19-2105G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3832123 | ||||||
| chr12:3832173
|
G | A | 95 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(92): Show | 140 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(137): Show |
intron_variant | MODIFIER | c.19-2155C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3832173 | ||||||
| chr12:3832190
|
G | A | 34 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(31): Show | 54 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.19-2172C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3832190 | ||||||
| chr12:3832249
|
C | A | 93 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(90): Show | 134 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(131): Show |
intron_variant | MODIFIER | c.19-2231G>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3832249 | ||||||
| chr12:3832281
|
T | C | 5 | a0001c0001t0019g0053a0001c0001t0019g0297a0001c0001t0019g0299others(2): Show | 6 | HG01346.hp1 HG02280.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.19-2263A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3832281 | ||||||
| chr12:3832400
|
A | G | 3 | a0001c0001t0009g0006a0001c0001t0009g0158a0001c0001t0072g0154 | 7 | HG01884.hp1 HG01891.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-2382T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3832400 | ||||||
| chr12:3832454
|
G | A | 1 | a0001c0001t0070g0139 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.19-2436C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3832454 | ||||||
| chr12:3832555
|
T | C | 1 | a0001c0001t0014g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.19-2537A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3832555 | ||||||
| chr12:3832557
|
A | C | 6 | a0001c0001t0011g0168a0001c0001t0014g0165a0001c0001t0014g0166others(3): Show | 6 | HG01192.hp1 HG01358.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.19-2539T>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3832557 | ||||||
| chr12:3832565
|
C | T | 3 | a0001c0001t0017g0010a0001c0001t0037g0054a0001c0001t0038g0055 | 6 | HG00323.hp1 HG00642.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.19-2547G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3832565 | ||||||
| chr12:3832626
|
A | C | 28 | a0001c0001t0003g0001a0001c0001t0003g0013a0001c0001t0003g0014others(25): Show | 46 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.19-2608T>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3832626 | ||||||
| chr12:3832648
|
G | C | 1 | a0001c0001t0004g0237 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.19-2630C>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3832648 | ||||||
| chr12:3832731
|
A | G | 2 | a0001c0001t0011g0049a0001c0001t0011g0264 | 3 | HG00323.hp2 HG06807.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.19-2713T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3832731 | ||||||
| chr12:3832948
|
C | A | 1 | a0001c0001t0007g0206 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.19-2930G>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3832948 | ||||||
| chr12:3833028
|
G | T | 1 | a0001c0001t0063g0148 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.19-3010C>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3833028 | ||||||
| chr12:3833030
|
G | A | 1 | a0001c0001t0002g0043 | 2 | HG02970.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.19-3012C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3833030 | ||||||
| chr12:3833052
|
T | C | 1 | a0001c0001t0063g0148 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.19-3034A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3833052 | ||||||
| chr12:3833116
|
A | G | 32 | a0001c0001t0007g0020a0001c0001t0007g0036a0001c0001t0007g0037others(29): Show | 41 | HG01106.hp1 HG01496.hp1 HG01934.hp1 others(38): Show |
intron_variant | MODIFIER | c.19-3098T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3833116 | ||||||
| chr12:3833159
|
T | A | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | NA19067.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.19-3141A>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3833159 | ||||||
| chr12:3833171
|
C | A | 1 | a0001c0001t0003g0105 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.19-3153G>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3833171 | ||||||
| chr12:3833203
|
C | T | 21 | a0001c0001t0002g0009a0001c0001t0002g0031a0001c0001t0002g0051others(18): Show | 28 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(25): Show |
intron_variant | MODIFIER | c.19-3185G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3833203 | ||||||
| chr12:3833326
|
G | A | 1 | a0001c0001t0011g0272 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.19-3308C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3833326 | ||||||
| chr12:3833376
|
G | A | 1 | a0001c0001t0056g0256 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.19-3358C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3833376 | ||||||
| chr12:3833417
|
C | A | 1 | a0001c0001t0003g0105 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.19-3399G>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3833417 | ||||||
| chr12:3833417
|
C | T | 170 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(167): Show | 245 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(242): Show |
intron_variant | MODIFIER | c.19-3399G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3833417 | ||||||
| chr12:3833500
|
A | T | 1 | a0001c0001t0002g0278 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.19-3482T>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3833500 | ||||||
| chr12:3833981
|
G | A | 1 | a0001c0001t0003g0106 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.19-3963C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3833981 | ||||||
| chr12:3834010
|
A | G | 15 | a0001c0001t0009g0006a0001c0001t0009g0032a0001c0001t0009g0153others(12): Show | 23 | HG00323.hp1 HG00642.hp1 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.19-3992T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3834010 | ||||||
| chr12:3834240
|
G | T | 1 | a0001c0001t0002g0278 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.19-4222C>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3834240 | ||||||
| chr12:3834355
|
G | A | 1 | a0001c0001t0006g0226 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.19-4337C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3834355 | ||||||
| chr12:3834534
|
C | T | 171 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(168): Show | 246 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(243): Show |
intron_variant | MODIFIER | c.19-4516G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3834534 | ||||||
| chr12:3834541
|
A | G | 1 | a0001c0001t0039g0056 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.19-4523T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3834541 | ||||||
| chr12:3834634
|
C | CA | 21 | a0001c0001t0001g0005a0001c0001t0001g0113a0001c0001t0001g0119others(18): Show | 30 | HG00738.hp2 HG01074.hp1 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.19-4617dupT | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3834634 | ||||||
| chr12:3834634
|
C | CAA | 23 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0019others(20): Show | 39 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.19-4618_19-4617dup others(2): Show |
PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3834634 | ||||||
| chr12:3834634
|
CA | C | 43 | a0001c0001t0002g0050a0001c0001t0002g0274a0001c0001t0002g0285others(40): Show | 53 | HG01106.hp1 HG01256.hp1 HG01496.hp1 others(50): Show |
intron_variant | MODIFIER | c.19-4617delT | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3834634 | ||||||
| chr12:3834704
|
G | C | 4 | a0001c0001t0006g0214a0001c0001t0006g0215a0001c0001t0006g0296others(1): Show | 4 | HG02135.hp2 NA18983.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-4686C>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3834704 | ||||||
| chr12:3834719
|
C | T | 5 | a0001c0001t0019g0053a0001c0001t0019g0297a0001c0001t0019g0299others(2): Show | 6 | HG01346.hp1 HG02280.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.19-4701G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3834719 | ||||||
| chr12:3834790
|
AGAG | A | 29 | a0001c0001t0005g0003a0001c0001t0005g0033a0001c0001t0005g0034others(26): Show | 41 | HG00639.hp2 HG01081.hp1 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.19-4775_19-4773del others(3): Show |
PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3834790 | ||||||
| chr12:3834810
|
A | G | 1 | a0001c0001t0032g0207 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.19-4792T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3834810 | ||||||
| chr12:3834856
|
G | A | 148 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(145): Show | 217 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(214): Show |
intron_variant | MODIFIER | c.19-4838C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3834856 | ||||||
| chr12:3834910
|
G | A | 3 | a0001c0001t0001g0133a0001c0001t0001g0135a0001c0001t0029g0134 | 3 | HG01109.hp1 HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.19-4892C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3834910 | ||||||
| chr12:3834922
|
T | C | 28 | a0001c0001t0002g0273a0001c0001t0011g0048a0001c0001t0011g0049others(25): Show | 39 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.19-4904A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3834922 | ||||||
| chr12:3834963
|
C | T | 1 | a0001c0001t0007g0020 | 3 | NA18978.hp1 NA18990.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.19-4945G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3834963 | ||||||
| chr12:3835143
|
C | A | 1 | a0001c0001t0062g0141 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.19-5125G>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3835143 | ||||||
| chr12:3835175
|
A | G | 1 | a0001c0001t0015g0012 | 4 | HG01952.hp2 HG02258.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-5157T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3835175 | ||||||
| chr12:3835221
|
T | A | 2 | a0001c0001t0001g0019a0001c0001t0001g0123 | 4 | HG00673.hp1 NA18940.hp2 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-5203A>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3835221 | ||||||
| chr12:3835250
|
T | C | 1 | a0001c0001t0010g0071 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.19-5232A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3835250 | ||||||
| chr12:3835284
|
G | A | 1 | a0001c0001t0050g0140 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.19-5266C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3835284 | ||||||
| chr12:3835371
|
CTGTTA | C | 110 | a0001c0001t0002g0273a0001c0001t0003g0001a0001c0001t0003g0013others(107): Show | 153 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.19-5358_19-5354del others(5): Show |
PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3835371 | ||||||
| chr12:3835379
|
T | A | 110 | a0001c0001t0002g0273a0001c0001t0003g0001a0001c0001t0003g0013others(107): Show | 153 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.19-5361A>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3835379 | ||||||
| chr12:3835460
|
C | T | 299 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(296): Show | 415 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(412): Show |
intron_variant | MODIFIER | c.19-5442G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3835460 | ||||||
| chr12:3835559
|
T | C | 111 | a0001c0001t0002g0273a0001c0001t0003g0001a0001c0001t0003g0013others(108): Show | 158 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.19-5541A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3835559 | ||||||
| chr12:3835572
|
C | G | 2 | a0001c0001t0034g0136a0001c0001t0034g0137 | 2 | HG02622.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.19-5554G>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3835572 | ||||||
| chr12:3835607
|
A | C | 1 | a0001c0001t0018g0196 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.19-5589T>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3835607 | ||||||
| chr12:3835609
|
G | A | 1 | a0001c0001t0010g0059 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.19-5591C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3835609 | ||||||
| chr12:3835616
|
A | T | 17 | a0001c0001t0002g0273a0001c0001t0011g0048a0001c0001t0011g0049others(14): Show | 23 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(20): Show |
intron_variant | MODIFIER | c.19-5598T>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3835616 | ||||||
| chr12:3835658
|
T | C | 116 | a0001c0001t0002g0273a0001c0001t0003g0001a0001c0001t0003g0013others(113): Show | 164 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.19-5640A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3835658 | ||||||
| chr12:3835951
|
G | A | 14 | a0001c0001t0009g0006a0001c0001t0009g0153a0001c0001t0009g0155others(11): Show | 21 | HG00323.hp1 HG00642.hp1 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.19-5933C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3835951 | ||||||
| chr12:3835973
|
A | G | 1 | a0001c0001t0062g0141 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.19-5955T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3835973 | ||||||
| chr12:3836072
|
T | C | 2 | a0001c0001t0001g0017a0001c0001t0001g0126 | 4 | NA19001.hp2 NA19078.hp2 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-6054A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3836072 | ||||||
| chr12:3836177
|
C | A | 1 | a0001c0001t0013g0205 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.19-6159G>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3836177 | ||||||
| chr12:3836246
|
T | C | 1 | a0001c0001t0050g0140 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.19-6228A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3836246 | ||||||
| chr12:3836318
|
C | G | 1 | a0001c0001t0050g0140 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.19-6300G>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3836318 | ||||||
| chr12:3836325
|
TA | T | 33 | a0001c0001t0007g0020a0001c0001t0007g0036a0001c0001t0007g0037others(30): Show | 43 | HG01106.hp1 HG01261.hp2 HG01358.hp1 others(40): Show |
intron_variant | MODIFIER | c.19-6308delT | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3836325 | ||||||
| chr12:3836336
|
C | CA | 42 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(39): Show | 67 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.19-6319dupT | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3836336 | ||||||
| chr12:3836372
|
T | A | 1 | a0001c0001t0008g0131 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.19-6354A>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3836372 | ||||||
| chr12:3836487
|
T | C | 1 | a0001c0001t0056g0256 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.19-6469A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3836487 | ||||||
| chr12:3836498
|
T | C | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG00544.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.19-6480A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3836498 | ||||||
| chr12:3836512
|
C | A | 112 | a0001c0001t0003g0001a0001c0001t0003g0013a0001c0001t0003g0014others(109): Show | 159 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.19-6494G>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3836512 | ||||||
| chr12:3836537
|
AG | A | 3 | a0001c0001t0009g0006a0001c0001t0009g0158a0001c0001t0072g0154 | 7 | HG01884.hp1 HG01891.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-6520delC | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3836537 | ||||||
| chr12:3836560
|
A | G | 1 | a0001c0001t0054g0263 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.19-6542T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3836560 | ||||||
| chr12:3836908
|
AAAGTGAG others(3): Show |
A | 1 | a0001c0001t0010g0072 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.19-6900_19-6891del others(10): Show |
PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3836908 | ||||||
| chr12:3836922
|
G | C | 1 | a0001c0001t0010g0072 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.19-6904C>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3836922 | ||||||
| chr12:3837018
|
C | G | 3 | a0001c0001t0014g0183a0001c0001t0015g0012a0001c0001t0015g0030 | 7 | HG01358.hp2 HG01952.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-7000G>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3837018 | ||||||
| chr12:3837350
|
C | T | 24 | a0001c0001t0011g0048a0001c0001t0011g0049a0001c0001t0011g0168others(21): Show | 34 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.19-7332G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3837350 | ||||||
| chr12:3837468
|
A | C | 22 | a0001c0001t0008g0295a0001c0001t0010g0027a0001c0001t0010g0059others(19): Show | 24 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.19-7450T>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3837468 | ||||||
| chr12:3837473
|
A | G | 1 | a0001c0001t0050g0140 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.19-7455T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3837473 | ||||||
| chr12:3837526
|
A | C | 1 | a0001c0001t0005g0033 | 2 | HG01255.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.19-7508T>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3837526 | ||||||
| chr12:3837537
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.19-7519C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3837537 | ||||||
| chr12:3837565
|
G | A | 1 | a0001c0001t0001g0126 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.19-7547C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3837565 | ||||||
| chr12:3837662
|
C | G | 108 | a0001c0001t0002g0043a0001c0001t0003g0001a0001c0001t0003g0013others(105): Show | 155 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.19-7644G>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3837662 | ||||||
| chr12:3837666
|
G | GA | 41 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(38): Show | 65 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.19-7649dupT | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3837666 | ||||||
| chr12:3837753
|
C | G | 186 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(183): Show | 271 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(268): Show |
intron_variant | MODIFIER | c.19-7735G>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3837753 | ||||||
| chr12:3837837
|
G | A | 1 | a0001c0001t0003g0100 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.19-7819C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3837837 | ||||||
| chr12:3838258
|
T | C | 115 | a0001c0001t0002g0043a0001c0001t0002g0273a0001c0001t0003g0001others(112): Show | 163 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.19-8240A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3838258 | ||||||
| chr12:3838414
|
A | C | 1 | a0001c0001t0032g0207 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.19-8396T>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3838414 | ||||||
| chr12:3838569
|
C | G | 22 | a0001c0001t0011g0048a0001c0001t0011g0049a0001c0001t0011g0168others(19): Show | 28 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(25): Show |
intron_variant | MODIFIER | c.19-8551G>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3838569 | ||||||
| chr12:3838719
|
C | A | 1 | a0001c0001t0008g0295 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.19-8701G>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3838719 | ||||||
| chr12:3838841
|
G | A | 1 | a0001c0001t0005g0179 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.19-8823C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3838841 | ||||||
| chr12:3838885
|
G | C | 1 | a0001c0001t0039g0056 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.19-8867C>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3838885 | ||||||
| chr12:3838911
|
C | T | 33 | a0001c0001t0007g0020a0001c0001t0007g0036a0001c0001t0007g0037others(30): Show | 42 | HG01106.hp1 HG01496.hp1 HG01934.hp1 others(39): Show |
intron_variant | MODIFIER | c.19-8893G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3838911 | ||||||
| chr12:3838918
|
C | A | 1 | a0001c0001t0004g0047 | 2 | NA18945.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.19-8900G>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3838918 | ||||||
| chr12:3838984
|
G | A | 5 | a0001c0001t0019g0053a0001c0001t0019g0297a0001c0001t0019g0299others(2): Show | 6 | HG01346.hp1 HG02280.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.19-8966C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3838984 | ||||||
| chr12:3839114
|
C | A | 2 | a0001c0001t0003g0014a0001c0001t0035g0097 | 4 | NA18942.hp2 NA18982.hp2 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-9096G>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3839114 | ||||||
| chr12:3839116
|
C | T | 113 | a0001c0001t0002g0116a0001c0001t0003g0001a0001c0001t0003g0013others(110): Show | 159 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.19-9098G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3839116 | ||||||
| chr12:3839161
|
C | CGCCGCCT | 22 | a0001c0001t0002g0009a0001c0001t0002g0031a0001c0001t0002g0051others(19): Show | 29 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.19-9150_19-9144dup others(7): Show |
PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3839161 | ||||||
| chr12:3839303
|
T | C | 1 | a0001c0001t0005g0171 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.19-9285A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3839303 | ||||||
| chr12:3839343
|
C | T | 2 | a0001c0001t0005g0209a0001c0001t0005g0229 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.19-9325G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3839343 | ||||||
| chr12:3839375
|
T | G | 2 | a0001c0001t0002g0273a0001c0001t0008g0052 | 3 | HG03688.hp1 HG04228.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.19-9357A>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3839375 | ||||||
| chr12:3839384
|
A | G | 120 | a0001c0001t0002g0043a0001c0001t0003g0001a0001c0001t0003g0013others(117): Show | 173 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.19-9366T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3839384 | ||||||
| chr12:3839453
|
C | T | 28 | a0001c0001t0003g0001a0001c0001t0003g0013a0001c0001t0003g0014others(25): Show | 46 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.19-9435G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3839453 | ||||||
| chr12:3839552
|
G | A | 271 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(268): Show | 378 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(375): Show |
intron_variant | MODIFIER | c.19-9534C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3839552 | ||||||
| chr12:3839682
|
T | C | 1 | a0001c0001t0005g0179 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.19-9664A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3839682 | ||||||
| chr12:3839875
|
G | C | 1 | a0001c0001t0010g0073 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.19-9857C>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3839875 | ||||||
| chr12:3839930
|
A | G | 1 | a0001c0001t0004g0023 | 3 | NA18968.hp1 NA18987.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.19-9912T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3839930 | ||||||
| chr12:3839935
|
A | G | 33 | a0001c0001t0007g0020a0001c0001t0007g0036a0001c0001t0007g0037others(30): Show | 43 | HG01106.hp1 HG01261.hp2 HG01358.hp1 others(40): Show |
intron_variant | MODIFIER | c.19-9917T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3839935 | ||||||
| chr12:3839965
|
G | A | 1 | a0001c0001t0034g0136 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.19-9947C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3839965 | ||||||
| chr12:3839994
|
G | C | 1 | a0001c0001t0063g0148 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.19-9976C>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3839994 | ||||||
| chr12:3840068
|
A | G | 1 | a0001c0001t0009g0032 | 2 | HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.19-10050T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3840068 | ||||||
| chr12:3840165
|
C | T | 2 | a0001c0001t0002g0043a0001c0001t0015g0012 | 6 | HG01952.hp2 HG02258.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.19-10147G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3840165 | ||||||
| chr12:3840226
|
C | G | 3 | a0001c0001t0033g0044a0001c0001t0064g0211a0001c0001t0065g0212 | 4 | HG02622.hp1 HG02976.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-10208G>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3840226 | ||||||
| chr12:3840332
|
T | A | 16 | a0001c0001t0002g0273a0001c0001t0011g0048a0001c0001t0011g0049others(13): Show | 22 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(19): Show |
intron_variant | MODIFIER | c.19-10314A>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3840332 | ||||||
| chr12:3840419
|
C | T | 1 | a0001c0001t0009g0158 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.19-10401G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3840419 | ||||||
| chr12:3840535
|
C | T | 6 | a0001c0001t0019g0053a0001c0001t0019g0297a0001c0001t0019g0299others(3): Show | 7 | HG01346.hp1 HG02280.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-10517G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3840535 | ||||||
| chr12:3840744
|
G | A | 2 | a0001c0001t0002g0022a0001c0001t0004g0232 | 4 | HG00738.hp2 HG01074.hp1 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-10726C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3840744 | ||||||
| chr12:3840749
|
A | C | 3 | a0001c0001t0033g0044a0001c0001t0064g0211a0001c0001t0065g0212 | 4 | HG02622.hp1 HG02976.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-10731T>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3840749 | ||||||
| chr12:3840992
|
C | T | 29 | a0001c0001t0005g0003a0001c0001t0005g0033a0001c0001t0005g0034others(26): Show | 41 | HG00639.hp2 HG01081.hp1 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.19-10974G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3840992 | ||||||
| chr12:3841016
|
G | T | 188 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(185): Show | 273 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(270): Show |
intron_variant | MODIFIER | c.19-10998C>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3841016 | ||||||
| chr12:3841018
|
C | T | 188 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(185): Show | 273 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(270): Show |
intron_variant | MODIFIER | c.19-11000G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3841018 | ||||||
| chr12:3841083
|
C | G | 27 | a0001c0001t0003g0001a0001c0001t0003g0013a0001c0001t0003g0014others(24): Show | 45 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.19-11065G>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3841083 | ||||||
| chr12:3841143
|
A | G | 1 | a0001c0001t0023g0161 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.19-11125T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3841143 | ||||||
| chr12:3841319
|
C | T | 2 | a0001c0001t0010g0065a0001c0001t0010g0066 | 2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.19-11301G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3841319 | ||||||
| chr12:3841410
|
T | G | 3 | a0001c0001t0016g0008a0001c0001t0016g0269a0001c0001t0075g0268 | 7 | HG00621.hp1 NA18612.hp2 NA18941.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-11392A>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3841410 | ||||||
| chr12:3841434
|
C | T | 1 | a0001c0001t0050g0140 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.19-11416G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3841434 | ||||||
| chr12:3841533
|
G | A | 5 | a0001c0001t0022g0185a0001c0001t0022g0187a0001c0001t0022g0188others(2): Show | 5 | HG02074.hp2 HG02132.hp2 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.19-11515C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3841533 | ||||||
| chr12:3841588
|
G | A | 1 | a0001c0001t0028g0035 | 2 | HG01261.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.19-11570C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3841588 | ||||||
| chr12:3841688
|
A | G | 1 | a0001c0001t0004g0240 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.19-11670T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3841688 | ||||||
| chr12:3841720
|
C | G | 1 | a0001c0001t0076g0284 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.19-11702G>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3841720 | ||||||
| chr12:3841760
|
A | G | 1 | a0001c0001t0021g0084 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.19-11742T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3841760 | ||||||
| chr12:3841811
|
T | C | 138 | a0001c0001t0002g0043a0001c0001t0002g0273a0001c0001t0003g0001others(135): Show | 197 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.19-11793A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3841811 | ||||||
| chr12:3841901
|
A | G | 2 | a0001c0001t0010g0065a0001c0001t0010g0066 | 2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.19-11883T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3841901 | ||||||
| chr12:3841956
|
G | C | 23 | a0001c0001t0002g0273a0001c0001t0011g0048a0001c0001t0011g0049others(20): Show | 29 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(26): Show |
intron_variant | MODIFIER | c.19-11938C>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3841956 | ||||||
| chr12:3841986
|
G | A | 1 | a0001c0001t0006g0223 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.19-11968C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3841986 | ||||||
| chr12:3842002
|
C | T | 1 | a0001c0001t0003g0092 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.19-11984G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3842002 | ||||||
| chr12:3842014
|
A | G | 1 | a0001c0001t0005g0179 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.19-11996T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3842014 | ||||||
| chr12:3842028
|
C | T | 22 | a0001c0001t0011g0048a0001c0001t0011g0049a0001c0001t0011g0168others(19): Show | 28 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(25): Show |
intron_variant | MODIFIER | c.19-12010G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3842028 | ||||||
| chr12:3842143
|
A | G | 111 | a0001c0001t0002g0043a0001c0001t0003g0001a0001c0001t0003g0013others(108): Show | 159 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.19-12125T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3842143 | ||||||
| chr12:3842291
|
A | T | 1 | a0001c0001t0001g0133 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.19-12273T>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3842291 | ||||||
| chr12:3842359
|
G | A | 1 | a0001c0001t0004g0231 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.19-12341C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3842359 | ||||||
| chr12:3842391
|
G | T | 27 | a0001c0001t0003g0001a0001c0001t0003g0013a0001c0001t0003g0014others(24): Show | 45 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.19-12373C>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3842391 | ||||||
| chr12:3842574
|
C | T | 1 | a0001c0001t0050g0140 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.19-12556G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3842574 | ||||||
| chr12:3842986
|
A | T | 3 | a0001c0001t0002g0043a0001c0001t0015g0012a0001c0001t0015g0030 | 8 | HG01952.hp2 HG02258.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.19-12968T>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3842986 | ||||||
| chr12:3843210
|
C | T | 29 | a0001c0001t0005g0003a0001c0001t0005g0033a0001c0001t0005g0034others(26): Show | 41 | HG00639.hp2 HG01081.hp1 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.19-13192G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3843210 | ||||||
| chr12:3843275
|
A | G | 35 | a0001c0001t0005g0003a0001c0001t0005g0033a0001c0001t0005g0034others(32): Show | 52 | HG00639.hp2 HG01081.hp1 HG01106.hp2 others(49): Show |
intron_variant | MODIFIER | c.19-13257T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3843275 | ||||||
| chr12:3843312
|
C | T | 1 | a0001c0001t0005g0143 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.19-13294G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3843312 | ||||||
| chr12:3843422
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.19-13404T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3843422 | ||||||
| chr12:3843522
|
C | T | 28 | a0001c0001t0003g0001a0001c0001t0003g0013a0001c0001t0003g0014others(25): Show | 46 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.19-13504G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3843522 | ||||||
| chr12:3843677
|
T | C | 1 | a0001c0001t0010g0074 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.19-13659A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3843677 | ||||||
| chr12:3843732
|
T | C | 28 | a0001c0001t0003g0001a0001c0001t0003g0013a0001c0001t0003g0014others(25): Show | 46 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.19-13714A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3843732 | ||||||
| chr12:3843931
|
A | G | 1 | a0001c0001t0070g0139 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.19-13913T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3843931 | ||||||
| chr12:3844069
|
C | A | 1 | a0001c0001t0063g0148 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.19-14051G>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3844069 | ||||||
| chr12:3844159
|
G | A | 1 | a0001c0001t0002g0280 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.19-14141C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3844159 | ||||||
| chr12:3844247
|
A | G | 2 | a0001c0001t0034g0136a0001c0001t0034g0137 | 2 | HG02622.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.19-14229T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3844247 | ||||||
| chr12:3844270
|
G | A | 2 | a0001c0001t0069g0147a0001c0001t0070g0139 | 2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.19-14252C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3844270 | ||||||
| chr12:3844352
|
T | G | 1 | a0001c0001t0028g0035 | 2 | HG01261.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.19-14334A>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3844352 | ||||||
| chr12:3844422
|
C | T | 1 | a0001c0001t0071g0230 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.19-14404G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3844422 | ||||||
| chr12:3844529
|
A | T | 5 | a0001c0001t0011g0168a0001c0001t0014g0165a0001c0001t0014g0166others(2): Show | 5 | HG01192.hp1 HG01891.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.19-14511T>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3844529 | ||||||
| chr12:3844530
|
T | G | 5 | a0001c0001t0011g0168a0001c0001t0014g0165a0001c0001t0014g0166others(2): Show | 5 | HG01192.hp1 HG01891.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.19-14512A>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3844530 | ||||||
| chr12:3844752
|
T | C | 56 | a0001c0001t0006g0004a0001c0001t0006g0021a0001c0001t0006g0045others(53): Show | 74 | HG00408.hp1 HG00544.hp2 HG01106.hp1 others(71): Show |
intron_variant | MODIFIER | c.19-14734A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3844752 | ||||||
| chr12:3844774
|
C | T | 133 | a0001c0001t0003g0001a0001c0001t0003g0013a0001c0001t0003g0014others(130): Show | 187 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.19-14756G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3844774 | ||||||
| chr12:3844791
|
C | T | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG02523.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.19-14773G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3844791 | ||||||
| chr12:3844955
|
C | G | 1 | a0001c0001t0070g0139 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.19-14937G>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3844955 | ||||||
| chr12:3844976
|
T | C | 1 | a0001c0001t0004g0249 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.19-14958A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3844976 | ||||||
| chr12:3845020
|
A | C | 4 | a0001c0001t0014g0165a0001c0001t0014g0166a0001c0001t0014g0169others(1): Show | 4 | HG01192.hp1 HG01358.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-15002T>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3845020 | ||||||
| chr12:3845046
|
TCAC | T | 106 | a0001c0001t0002g0273a0001c0001t0003g0001a0001c0001t0003g0013others(103): Show | 148 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.19-15031_19-15029d others(5): Show |
PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3845046 | ||||||
| chr12:3845307
|
T | C | 28 | a0001c0001t0003g0001a0001c0001t0003g0013a0001c0001t0003g0014others(25): Show | 46 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.19-15289A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3845307 | ||||||
| chr12:3845367
|
C | T | 141 | a0001c0001t0002g0043a0001c0001t0002g0273a0001c0001t0003g0001others(138): Show | 201 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.19-15349G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3845367 | ||||||
| chr12:3845390
|
T | C | 112 | a0001c0001t0002g0043a0001c0001t0002g0273a0001c0001t0003g0001others(109): Show | 160 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.19-15372A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3845390 | ||||||
| chr12:3845432
|
C | G | 1 | a0001c0001t0069g0147 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.19-15414G>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3845432 | ||||||
| chr12:3845473
|
T | C | 141 | a0001c0001t0002g0043a0001c0001t0002g0273a0001c0001t0003g0001others(138): Show | 201 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.19-15455A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3845473 | ||||||
| chr12:3845572
|
A | G | 32 | a0001c0001t0007g0020a0001c0001t0007g0036a0001c0001t0007g0037others(29): Show | 41 | HG01106.hp1 HG01496.hp1 HG01934.hp1 others(38): Show |
intron_variant | MODIFIER | c.19-15554T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3845572 | ||||||
| chr12:3845636
|
C | T | 5 | a0001c0001t0007g0037a0001c0001t0007g0192a0001c0001t0007g0195others(2): Show | 6 | HG02056.hp2 NA18747.hp1 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.19-15618G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3845636 | ||||||
| chr12:3845648
|
C | T | 1 | a0001c0001t0028g0035 | 2 | HG01261.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.19-15630G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3845648 | ||||||
| chr12:3845795
|
TAATTGGG others(4): Show |
T | 1 | a0001c0001t0009g0158 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.19-15788_19-15778d others(13): Show |
PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3845795 | ||||||
| chr12:3845973
|
C | T | 1 | a0001c0001t0003g0089 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.19-15955G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3845973 | ||||||
| chr12:3846068
|
AT | A | 5 | a0001c0001t0019g0053a0001c0001t0019g0297a0001c0001t0019g0299others(2): Show | 6 | HG01346.hp1 HG02280.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.19-16051delA | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3846068 | ||||||
| chr12:3846093
|
T | C | 141 | a0001c0001t0002g0043a0001c0001t0002g0273a0001c0001t0003g0001others(138): Show | 201 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.19-16075A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3846093 | ||||||
| chr12:3846271
|
A | AT | 5 | a0001c0001t0019g0053a0001c0001t0019g0297a0001c0001t0019g0299others(2): Show | 6 | HG01346.hp1 HG02280.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.19-16254dupA | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3846271 | ||||||
| chr12:3846275
|
A | C | 1 | a0001c0001t0050g0140 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.19-16257T>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3846275 | ||||||
| chr12:3846320
|
G | T | 1 | a0001c0001t0063g0148 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.19-16302C>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3846320 | ||||||
| chr12:3846394
|
T | C | 1 | a0001c0001t0005g0179 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.19-16376A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3846394 | ||||||
| chr12:3846475
|
G | A | 1 | a0001c0001t0009g0157 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.19-16457C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3846475 | ||||||
| chr12:3846573
|
G | A | 4 | a0001c0001t0009g0153a0001c0001t0009g0155a0001c0001t0009g0157others(1): Show | 4 | HG02451.hp2 HG02809.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-16555C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3846573 | ||||||
| chr12:3846584
|
G | A | 40 | a0001c0001t0002g0022a0001c0001t0002g0024a0001c0001t0002g0239others(37): Show | 52 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.19-16566C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3846584 | ||||||
| chr12:3846663
|
A | C | 28 | a0001c0001t0003g0001a0001c0001t0003g0013a0001c0001t0003g0014others(25): Show | 46 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.19-16645T>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3846663 | ||||||
| chr12:3846669
|
A | G | 1 | a0001c0001t0008g0130 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.19-16651T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3846669 | ||||||
| chr12:3846673
|
C | T | 32 | a0001c0001t0007g0020a0001c0001t0007g0036a0001c0001t0007g0037others(29): Show | 41 | HG01106.hp1 HG01496.hp1 HG01934.hp1 others(38): Show |
intron_variant | MODIFIER | c.19-16655G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3846673 | ||||||
| chr12:3846713
|
C | T | 1 | a0001c0001t0009g0153 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.19-16695G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3846713 | ||||||
| chr12:3846716
|
C | T | 23 | a0001c0001t0002g0273a0001c0001t0011g0048a0001c0001t0011g0049others(20): Show | 29 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(26): Show |
intron_variant | MODIFIER | c.19-16698G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3846716 | ||||||
| chr12:3846756
|
TA | T | 7 | a0001c0001t0002g0239a0001c0001t0004g0238a0001c0001t0005g0172others(4): Show | 7 | HG00639.hp1 HG01168.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-16739delT | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3846756 | ||||||
| chr12:3846779
|
A | AAAAG | 141 | a0001c0001t0002g0043a0001c0001t0002g0273a0001c0001t0003g0001others(138): Show | 201 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.19-16762_19-16761i others(6): Show |
PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3846779 | ||||||
| chr12:3846788
|
T | C | 16 | a0001c0001t0004g0160a0001c0001t0009g0006a0001c0001t0009g0032others(13): Show | 24 | HG00323.hp1 HG00642.hp1 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.19-16770A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3846788 | ||||||
| chr12:3846795
|
C | T | 1 | a0001c0001t0050g0140 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.19-16777G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3846795 | ||||||
| chr12:3846873
|
C | T | 1 | a0001c0001t0003g0107 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.19-16855G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3846873 | ||||||
| chr12:3846948
|
G | A | 1 | a0001c0001t0002g0250 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.19-16930C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3846948 | ||||||
| chr12:3846994
|
C | T | 105 | a0001c0001t0002g0273a0001c0001t0003g0001a0001c0001t0003g0013others(102): Show | 147 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.19-16976G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3846994 | ||||||
| chr12:3847155
|
A | G | 21 | a0001c0001t0006g0004a0001c0001t0006g0021a0001c0001t0006g0045others(18): Show | 29 | HG00408.hp1 HG00544.hp2 HG02135.hp2 others(26): Show |
intron_variant | MODIFIER | c.19-17137T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3847155 | ||||||
| chr12:3847183
|
T | C | 4 | a0001c0001t0005g0040a0001c0001t0005g0041a0001c0001t0005g0042others(1): Show | 7 | HG01884.hp2 HG02257.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-17165A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3847183 | ||||||
| chr12:3847402
|
T | C | 1 | a0001c0001t0009g0158 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.19-17384A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3847402 | ||||||
| chr12:3847589
|
T | C | 1 | a0001c0001t0005g0178 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.19-17571A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3847589 | ||||||
| chr12:3848008
|
T | C | 21 | a0001c0001t0006g0004a0001c0001t0006g0021a0001c0001t0006g0045others(18): Show | 29 | HG00408.hp1 HG00544.hp2 HG02135.hp2 others(26): Show |
intron_variant | MODIFIER | c.19-17990A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3848008 | ||||||
| chr12:3848098
|
A | G | 1 | a0001c0001t0007g0190 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.19-18080T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3848098 | ||||||
| chr12:3848302
|
G | A | 1 | a0001c0001t0050g0140 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.19-18284C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3848302 | ||||||
| chr12:3848378
|
A | G | 187 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(184): Show | 273 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(270): Show |
intron_variant | MODIFIER | c.19-18360T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3848378 | ||||||
| chr12:3848538
|
C | T | 1 | a0001c0001t0028g0035 | 2 | HG01261.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.19-18520G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3848538 | ||||||
| chr12:3848655
|
A | C | 1 | a0001c0001t0006g0218 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.19-18637T>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3848655 | ||||||
| chr12:3848661
|
A | G | 1 | a0001c0001t0050g0140 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.19-18643T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3848661 | ||||||
| chr12:3848718
|
C | T | 1 | a0001c0001t0050g0140 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.19-18700G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3848718 | ||||||
| chr12:3848961
|
GA | G | 12 | a0001c0001t0002g0043a0001c0001t0010g0075a0001c0001t0011g0168others(9): Show | 17 | HG01192.hp1 HG01358.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.19-18944delT | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3848961 | ||||||
| chr12:3848966
|
A | G | 1 | a0001c0001t0006g0219 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.19-18948T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3848966 | ||||||
| chr12:3848970
|
A | C | 2 | a0001c0001t0005g0181a0001c0001t0005g0182 | 2 | NA18957.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.19-18952T>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3848970 | ||||||
| chr12:3848996
|
G | T | 1 | a0001c0001t0007g0192 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.19-18978C>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3848996 | ||||||
| chr12:3849053
|
T | C | 40 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(37): Show | 64 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.19-19035A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3849053 | ||||||
| chr12:3849075
|
A | G | 33 | a0001c0001t0007g0020a0001c0001t0007g0036a0001c0001t0007g0037others(30): Show | 43 | HG01106.hp1 HG01261.hp2 HG01358.hp1 others(40): Show |
intron_variant | MODIFIER | c.19-19057T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3849075 | ||||||
| chr12:3849113
|
A | G | 28 | a0001c0001t0002g0031a0001c0001t0003g0001a0001c0001t0003g0013others(25): Show | 47 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.19-19095T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3849113 | ||||||
| chr12:3849198
|
G | A | 1 | a0001c0001t0052g0291 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.19-19180C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3849198 | ||||||
| chr12:3849258
|
C | CA | 9 | a0001c0001t0002g0043a0001c0001t0011g0168a0001c0001t0014g0165others(6): Show | 14 | HG01192.hp1 HG01358.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.19-19241dupT | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3849258 | ||||||
| chr12:3849296
|
A | G | 16 | a0001c0001t0011g0048a0001c0001t0011g0049a0001c0001t0011g0264others(13): Show | 22 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(19): Show |
intron_variant | MODIFIER | c.19-19278T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3849296 | ||||||
| chr12:3849297
|
C | T | 1 | a0001c0001t0031g0191 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.19-19279G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3849297 | ||||||
| chr12:3849322
|
A | C | 1 | a0001c0001t0001g0129 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.19-19304T>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3849322 | ||||||
| chr12:3849447
|
A | T | 1 | a0001c0001t0007g0036 | 2 | HG02015.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.19-19429T>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3849447 | ||||||
| chr12:3849487
|
T | C | 1 | a0001c0001t0004g0255 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.19-19469A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3849487 | ||||||
| chr12:3849533
|
A | G | 1 | a0001c0001t0006g0218 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.19-19515T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3849533 | ||||||
| chr12:3849547
|
A | G | 231 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(228): Show | 327 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(324): Show |
intron_variant | MODIFIER | c.19-19529T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3849547 | ||||||
| chr12:3849643
|
G | A | 92 | a0001c0001t0002g0031a0001c0001t0002g0043a0001c0001t0003g0001others(89): Show | 134 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(131): Show |
intron_variant | MODIFIER | c.19-19625C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3849643 | ||||||
| chr12:3849697
|
A | G | 1 | a0001c0001t0012g0076 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.19-19679T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3849697 | ||||||
| chr12:3849724
|
A | G | 2 | a0001c0001t0004g0254a0001c0001t0047g0253 | 2 | HG00642.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.19-19706T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3849724 | ||||||
| chr12:3849761
|
T | C | 1 | a0001c0001t0009g0159 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.19-19743A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3849761 | ||||||
| chr12:3849768
|
A | G | 1 | a0001c0001t0007g0190 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.19-19750T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3849768 | ||||||
| chr12:3849938
|
T | C | 1 | a0001c0001t0034g0137 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.19-19920A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3849938 | ||||||
| chr12:3849946
|
G | A | 5 | a0001c0001t0019g0053a0001c0001t0019g0297a0001c0001t0019g0299others(2): Show | 6 | HG01346.hp1 HG02280.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.19-19928C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3849946 | ||||||
| chr12:3849960
|
TTTTTAAA others(11): Show |
T | 1 | a0001c0001t0010g0059 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.19-19960_19-19943d others(20): Show |
PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3849960 | ||||||
| chr12:3850309
|
C | T | 2 | a0001c0001t0034g0136a0001c0001t0034g0137 | 2 | HG02622.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.19-20291G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3850309 | ||||||
| chr12:3850533
|
C | T | 1 | a0001c0001t0004g0237 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.19-20515G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3850533 | ||||||
| chr12:3850760
|
T | C | 1 | a0001c0001t0001g0127 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.19-20742A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3850760 | ||||||
| chr12:3850761
|
C | CTT | 31 | a0001c0001t0007g0020a0001c0001t0007g0036a0001c0001t0007g0037others(28): Show | 40 | HG01106.hp1 HG01496.hp1 HG01934.hp1 others(37): Show |
intron_variant | MODIFIER | c.19-20744_19-20743i others(4): Show |
PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3850761 | ||||||
| chr12:3850797
|
A | G | 186 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(183): Show | 272 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(269): Show |
intron_variant | MODIFIER | c.19-20779T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3850797 | ||||||
| chr12:3850808
|
A | G | 1 | a0001c0001t0004g0236 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.19-20790T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3850808 | ||||||
| chr12:3850888
|
A | G | 2 | a0001c0001t0010g0027a0001c0001t0010g0064 | 3 | HG02165.hp1 NA18953.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.19-20870T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3850888 | ||||||
| chr12:3851006
|
G | A | 1 | a0001c0001t0071g0230 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.19-20988C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3851006 | ||||||
| chr12:3851186
|
G | A | 11 | a0001c0001t0002g0116a0001c0001t0008g0016a0001c0001t0008g0018others(8): Show | 15 | HG01169.hp1 HG02055.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.19-21168C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3851186 | ||||||
| chr12:3851257
|
T | C | 1 | a0001c0001t0008g0295 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.19-21239A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3851257 | ||||||
| chr12:3851265
|
C | G | 1 | a0001c0001t0001g0133 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.19-21247G>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3851265 | ||||||
| chr12:3851341
|
T | G | 1 | a0001c0001t0063g0148 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.19-21323A>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3851341 | ||||||
| chr12:3851445
|
C | T | 1 | a0001c0001t0005g0171 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.19-21427G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3851445 | ||||||
| chr12:3851476
|
G | A | 5 | a0001c0001t0019g0053a0001c0001t0019g0297a0001c0001t0019g0299others(2): Show | 6 | HG01346.hp1 HG02280.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.19-21458C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3851476 | ||||||
| chr12:3851522
|
G | A | 3 | a0001c0001t0004g0251a0001c0001t0021g0083a0001c0001t0061g0235 | 3 | HG01069.hp2 HG01175.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.19-21504C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3851522 | ||||||
| chr12:3851586
|
T | C | 5 | a0001c0001t0019g0053a0001c0001t0019g0297a0001c0001t0019g0299others(2): Show | 6 | HG01346.hp1 HG02280.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.19-21568A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3851586 | ||||||
| chr12:3851587
|
A | G | 24 | a0001c0001t0003g0100a0001c0001t0008g0295a0001c0001t0010g0027others(21): Show | 26 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.19-21569T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3851587 | ||||||
| chr12:3851654
|
C | T | 1 | a0001c0001t0005g0040 | 2 | HG02280.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.18+21558G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3851654 | ||||||
| chr12:3851676
|
G | C | 4 | a0001c0001t0011g0270a0001c0001t0011g0271a0001c0001t0011g0272others(1): Show | 4 | HG02698.hp2 HG03654.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+21536C>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3851676 | ||||||
| chr12:3851731
|
G | A | 1 | a0001c0001t0004g0252 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.18+21481C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3851731 | ||||||
| chr12:3851847
|
C | T | 27 | a0001c0001t0003g0001a0001c0001t0003g0013a0001c0001t0003g0014others(24): Show | 45 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.18+21365G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3851847 | ||||||
| chr12:3851882
|
G | C | 1 | a0001c0001t0021g0084 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.18+21330C>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3851882 | ||||||
| chr12:3851885
|
G | A | 2 | a0001c0001t0069g0147a0001c0001t0070g0139 | 2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.18+21327C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3851885 | ||||||
| chr12:3852032
|
A | C | 5 | a0001c0001t0022g0185a0001c0001t0022g0187a0001c0001t0022g0188others(2): Show | 5 | HG02074.hp2 HG02132.hp2 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+21180T>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3852032 | ||||||
| chr12:3852096
|
A | G | 1 | a0001c0001t0001g0111 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.18+21116T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3852096 | ||||||
| chr12:3852136
|
G | A | 29 | a0001c0001t0005g0003a0001c0001t0005g0033a0001c0001t0005g0034others(26): Show | 41 | HG00639.hp2 HG01081.hp1 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.18+21076C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3852136 | ||||||
| chr12:3852166
|
C | T | 1 | a0001c0001t0063g0148 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.18+21046G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3852166 | ||||||
| chr12:3852196
|
C | T | 1 | a0001c0001t0006g0045 | 2 | NA18970.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.18+21016G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3852196 | ||||||
| chr12:3852303
|
G | A | 1 | a0001c0001t0003g0014 | 3 | NA18982.hp2 NA19063.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.18+20909C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3852303 | ||||||
| chr12:3852338
|
C | T | 1 | a0001c0001t0003g0089 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.18+20874G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3852338 | ||||||
| chr12:3852402
|
G | A | 40 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(37): Show | 64 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.18+20810C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3852402 | ||||||
| chr12:3852449
|
T | C | 1 | a0001c0001t0006g0224 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.18+20763A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3852449 | ||||||
| chr12:3852537
|
A | G | 3 | a0001c0001t0033g0044a0001c0001t0064g0211a0001c0001t0065g0212 | 4 | HG02622.hp1 HG02976.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+20675T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3852537 | ||||||
| chr12:3852737
|
A | G | 3 | a0001c0001t0002g0281a0001c0001t0002g0283a0001c0001t0004g0282 | 3 | HG00099.hp2 HG01243.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.18+20475T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3852737 | ||||||
| chr12:3852761
|
A | C | 1 | a0001c0001t0002g0280 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.18+20451T>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3852761 | ||||||
| chr12:3852805
|
C | T | 1 | a0001c0001t0004g0261 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.18+20407G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3852805 | ||||||
| chr12:3852879
|
G | C | 6 | a0001c0001t0011g0168a0001c0001t0014g0165a0001c0001t0014g0166others(3): Show | 6 | HG01192.hp1 HG01358.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+20333C>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3852879 | ||||||
| chr12:3853190
|
G | A | 1 | a0001c0001t0003g0146 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.18+20022C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3853190 | ||||||
| chr12:3853269
|
G | A | 1 | a0001c0001t0010g0075 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.18+19943C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3853269 | ||||||
| chr12:3853315
|
C | T | 1 | a0001c0001t0050g0140 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.18+19897G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3853315 | ||||||
| chr12:3853436
|
G | A | 91 | a0001c0001t0002g0043a0001c0001t0003g0001a0001c0001t0003g0013others(88): Show | 132 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.18+19776C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3853436 | ||||||
| chr12:3853596
|
A | G | 1 | a0001c0001t0008g0279 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.18+19616T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3853596 | ||||||
| chr12:3853599
|
T | C | 1 | a0001c0001t0004g0160 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.18+19613A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3853599 | ||||||
| chr12:3853602
|
G | C | 1 | a0001c0001t0002g0138 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.18+19610C>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3853602 | ||||||
| chr12:3853720
|
G | C | 21 | a0001c0001t0006g0004a0001c0001t0006g0021a0001c0001t0006g0045others(18): Show | 29 | HG00408.hp1 HG00544.hp2 HG02135.hp2 others(26): Show |
intron_variant | MODIFIER | c.18+19492C>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3853720 | ||||||
| chr12:3853726
|
C | T | 1 | a0001c0001t0005g0041 | 2 | HG01884.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.18+19486G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3853726 | ||||||
| chr12:3853797
|
T | C | 27 | a0001c0001t0003g0001a0001c0001t0003g0013a0001c0001t0003g0014others(24): Show | 45 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.18+19415A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3853797 | ||||||
| chr12:3853876
|
T | C | 1 | a0001c0001t0002g0273 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.18+19336A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3853876 | ||||||
| chr12:3854027
|
A | G | 5 | a0001c0001t0034g0136a0001c0001t0034g0137a0001c0001t0069g0147others(2): Show | 5 | HG02615.hp2 HG02622.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.18+19185T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3854027 | ||||||
| chr12:3854143
|
G | A | 1 | a0001c0001t0071g0230 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.18+19069C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3854143 | ||||||
| chr12:3854199
|
G | A | 1 | a0001c0001t0063g0148 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.18+19013C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3854199 | ||||||
| chr12:3854229
|
C | G | 91 | a0001c0001t0002g0043a0001c0001t0003g0001a0001c0001t0003g0013others(88): Show | 132 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.18+18983G>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3854229 | ||||||
| chr12:3854262
|
A | G | 4 | a0001c0001t0014g0165a0001c0001t0014g0166a0001c0001t0014g0169others(1): Show | 4 | HG01192.hp1 HG01358.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+18950T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3854262 | ||||||
| chr12:3854274
|
A | G | 1 | a0001c0001t0006g0296 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.18+18938T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3854274 | ||||||
| chr12:3854301
|
G | A | 91 | a0001c0001t0002g0043a0001c0001t0003g0001a0001c0001t0003g0013others(88): Show | 132 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.18+18911C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3854301 | ||||||
| chr12:3854310
|
G | A | 190 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(187): Show | 277 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(274): Show |
intron_variant | MODIFIER | c.18+18902C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3854310 | ||||||
| chr12:3854374
|
T | C | 21 | a0001c0001t0006g0004a0001c0001t0006g0021a0001c0001t0006g0045others(18): Show | 29 | HG00408.hp1 HG00544.hp2 HG02135.hp2 others(26): Show |
intron_variant | MODIFIER | c.18+18838A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3854374 | ||||||
| chr12:3854598
|
T | C | 1 | a0001c0001t0023g0163 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.18+18614A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3854598 | ||||||
| chr12:3854603
|
G | A | 1 | a0001c0001t0011g0049 | 2 | HG00323.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.18+18609C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3854603 | ||||||
| chr12:3854757
|
G | A | 2 | a0001c0001t0004g0254a0001c0001t0047g0253 | 2 | HG00642.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.18+18455C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3854757 | ||||||
| chr12:3854827
|
A | C | 2 | a0001c0001t0002g0031a0001c0001t0003g0145 | 3 | NA18969.hp1 NA18971.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.18+18385T>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3854827 | ||||||
| chr12:3855185
|
G | C | 1 | a0001c0001t0007g0206 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.18+18027C>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3855185 | ||||||
| chr12:3855357
|
A | T | 2 | a0001c0001t0005g0041a0001c0001t0005g0210 | 3 | HG01884.hp2 HG02257.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.18+17855T>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3855357 | ||||||
| chr12:3855470
|
G | A | 5 | a0001c0001t0019g0053a0001c0001t0019g0297a0001c0001t0019g0299others(2): Show | 6 | HG01346.hp1 HG02280.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+17742C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3855470 | ||||||
| chr12:3855509
|
T | G | 6 | a0001c0001t0011g0168a0001c0001t0014g0165a0001c0001t0014g0166others(3): Show | 6 | HG01192.hp1 HG01358.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+17703A>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3855509 | ||||||
| chr12:3855680
|
C | T | 33 | a0001c0001t0002g0278a0001c0001t0007g0020a0001c0001t0007g0036others(30): Show | 42 | HG01106.hp1 HG01496.hp1 HG01934.hp1 others(39): Show |
intron_variant | MODIFIER | c.18+17532G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3855680 | ||||||
| chr12:3855721
|
A | G | 1 | a0001c0001t0023g0161 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.18+17491T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3855721 | ||||||
| chr12:3856009
|
C | T | 32 | a0001c0001t0007g0020a0001c0001t0007g0036a0001c0001t0007g0037others(29): Show | 41 | HG01106.hp1 HG01496.hp1 HG01934.hp1 others(38): Show |
intron_variant | MODIFIER | c.18+17203G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3856009 | ||||||
| chr12:3856104
|
C | T | 1 | a0001c0001t0012g0061 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.18+17108G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3856104 | ||||||
| chr12:3856135
|
C | A | 32 | a0001c0001t0007g0020a0001c0001t0007g0036a0001c0001t0007g0037others(29): Show | 41 | HG01106.hp1 HG01496.hp1 HG01934.hp1 others(38): Show |
intron_variant | MODIFIER | c.18+17077G>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3856135 | ||||||
| chr12:3856197
|
T | C | 1 | a0001c0001t0007g0206 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.18+17015A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3856197 | ||||||
| chr12:3856329
|
G | C | 1 | a0001c0001t0001g0113 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.18+16883C>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3856329 | ||||||
| chr12:3856399
|
C | T | 3 | a0001c0001t0001g0133a0001c0001t0001g0135a0001c0001t0029g0134 | 3 | HG01109.hp1 HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.18+16813G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3856399 | ||||||
| chr12:3856415
|
A | G | 110 | a0001c0001t0002g0031a0001c0001t0002g0043a0001c0001t0002g0273others(107): Show | 158 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.18+16797T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3856415 | ||||||
| chr12:3856447
|
A | G | 1 | a0001c0001t0008g0295 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.18+16765T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3856447 | ||||||
| chr12:3856667
|
T | C | 2 | a0001c0001t0034g0136a0001c0001t0034g0137 | 2 | HG02622.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.18+16545A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3856667 | ||||||
| chr12:3856695
|
T | C | 1 | a0001c0001t0063g0148 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.18+16517A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3856695 | ||||||
| chr12:3856699
|
G | A | 21 | a0001c0001t0006g0004a0001c0001t0006g0021a0001c0001t0006g0045others(18): Show | 29 | HG00408.hp1 HG00544.hp2 HG02135.hp2 others(26): Show |
intron_variant | MODIFIER | c.18+16513C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3856699 | ||||||
| chr12:3856714
|
C | G | 142 | a0001c0001t0002g0031a0001c0001t0002g0043a0001c0001t0003g0001others(139): Show | 203 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.18+16498G>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3856714 | ||||||
| chr12:3856745
|
A | T | 1 | a0001c0001t0005g0170 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.18+16467T>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3856745 | ||||||
| chr12:3856796
|
A | G | 109 | a0001c0001t0002g0031a0001c0001t0002g0043a0001c0001t0003g0001others(106): Show | 157 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.18+16416T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3856796 | ||||||
| chr12:3856941
|
T | G | 1 | a0001c0001t0001g0128 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.18+16271A>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3856941 | ||||||
| chr12:3857045
|
G | A | 1 | a0001c0001t0006g0225 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.18+16167C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3857045 | ||||||
| chr12:3857125
|
C | A | 2 | a0001c0001t0003g0100a0001c0001t0004g0255 | 2 | HG02630.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.18+16087G>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3857125 | ||||||
| chr12:3857133
|
G | C | 5 | a0001c0001t0005g0040a0001c0001t0005g0041a0001c0001t0005g0042others(2): Show | 8 | HG01884.hp2 HG02257.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.18+16079C>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3857133 | ||||||
| chr12:3857242
|
G | A | 1 | a0001c0001t0027g0079 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.18+15970C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3857242 | ||||||
| chr12:3857257
|
C | T | 3 | a0001c0001t0033g0044a0001c0001t0064g0211a0001c0001t0065g0212 | 4 | HG02622.hp1 HG02976.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+15955G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3857257 | ||||||
| chr12:3857288
|
A | T | 3 | a0001c0001t0002g0277a0001c0001t0008g0295a0001c0001t0063g0148 | 3 | HG00438.hp2 HG03209.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.18+15924T>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3857288 | ||||||
| chr12:3857422
|
T | C | 1 | a0001c0001t0056g0256 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.18+15790A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3857422 | ||||||
| chr12:3857637
|
T | TA | 31 | a0001c0001t0002g0031a0001c0001t0003g0001a0001c0001t0003g0013others(28): Show | 50 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.18+15574dupT | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3857637 | ||||||
| chr12:3857784
|
A | G | 24 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0019others(21): Show | 40 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.18+15428T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3857784 | ||||||
| chr12:3858347
|
C | A | 40 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(37): Show | 64 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.18+14865G>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3858347 | ||||||
| chr12:3858545
|
G | A | 1 | a0001c0001t0005g0178 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.18+14667C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3858545 | ||||||
| chr12:3858612
|
G | A | 1 | a0001c0001t0005g0182 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.18+14600C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3858612 | ||||||
| chr12:3858671
|
T | C | 1 | a0001c0001t0028g0035 | 2 | HG01261.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.18+14541A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3858671 | ||||||
| chr12:3858818
|
G | A | 5 | a0001c0001t0002g0050a0001c0001t0002g0274a0001c0001t0002g0292others(2): Show | 7 | HG01433.hp1 NA18952.hp1 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.18+14394C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3858818 | ||||||
| chr12:3859066
|
C | T | 1 | a0001c0001t0003g0088 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.18+14146G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3859066 | ||||||
| chr12:3859077
|
G | A | 88 | a0001c0001t0002g0031a0001c0001t0003g0001a0001c0001t0003g0013others(85): Show | 125 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.18+14135C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3859077 | ||||||
| chr12:3859086
|
A | C | 9 | a0001c0001t0002g0116a0001c0001t0008g0016a0001c0001t0008g0018others(6): Show | 13 | HG01169.hp1 HG02055.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.18+14126T>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3859086 | ||||||
| chr12:3859165
|
A | G | 88 | a0001c0001t0002g0031a0001c0001t0003g0001a0001c0001t0003g0013others(85): Show | 125 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.18+14047T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3859165 | ||||||
| chr12:3859285
|
G | C | 1 | a0001c0001t0003g0098 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.18+13927C>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3859285 | ||||||
| chr12:3859288
|
G | A | 1 | a0001c0001t0005g0179 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.18+13924C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3859288 | ||||||
| chr12:3859304
|
T | A | 1 | a0001c0001t0014g0169 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.18+13908A>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3859304 | ||||||
| chr12:3859331
|
G | A | 1 | a0001c0001t0008g0110 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.18+13881C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3859331 | ||||||
| chr12:3859336
|
G | A | 88 | a0001c0001t0002g0031a0001c0001t0003g0001a0001c0001t0003g0013others(85): Show | 125 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.18+13876C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3859336 | ||||||
| chr12:3859368
|
A | T | 88 | a0001c0001t0002g0031a0001c0001t0003g0001a0001c0001t0003g0013others(85): Show | 125 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.18+13844T>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3859368 | ||||||
| chr12:3859381
|
G | A | 4 | a0001c0001t0006g0214a0001c0001t0006g0215a0001c0001t0006g0296others(1): Show | 4 | HG02135.hp2 NA18983.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+13831C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3859381 | ||||||
| chr12:3859391
|
T | C | 208 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(205): Show | 302 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(299): Show |
intron_variant | MODIFIER | c.18+13821A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3859391 | ||||||
| chr12:3859559
|
TA | T | 65 | a0001c0001t0002g0022a0001c0001t0002g0024a0001c0001t0002g0239others(62): Show | 87 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.18+13652delT | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3859559 | ||||||
| chr12:3859559
|
TAA | T | 68 | a0001c0001t0002g0031a0001c0001t0002g0138a0001c0001t0003g0001others(65): Show | 96 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(93): Show |
intron_variant | MODIFIER | c.18+13651_18+13652d others(4): Show |
PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3859559 | ||||||
| chr12:3859595
|
A | G | 2 | a0001c0001t0002g0043a0001c0001t0015g0012 | 6 | HG01952.hp2 HG02258.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.18+13617T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3859595 | ||||||
| chr12:3859690
|
T | G | 1 | a0001c0001t0014g0169 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.18+13522A>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3859690 | ||||||
| chr12:3859763
|
A | G | 1 | a0001c0001t0028g0035 | 2 | HG01261.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.18+13449T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3859763 | ||||||
| chr12:3859811
|
C | T | 40 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(37): Show | 64 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.18+13401G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3859811 | ||||||
| chr12:3859960
|
A | G | 92 | a0001c0001t0002g0031a0001c0001t0002g0043a0001c0001t0003g0001others(89): Show | 134 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(131): Show |
intron_variant | MODIFIER | c.18+13252T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3859960 | ||||||
| chr12:3859985
|
T | C | 1 | a0001c0001t0004g0258 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.18+13227A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3859985 | ||||||
| chr12:3859986
|
G | A | 1 | a0001c0001t0070g0139 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.18+13226C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3859986 | ||||||
| chr12:3860029
|
G | C | 24 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0019others(21): Show | 40 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.18+13183C>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3860029 | ||||||
| chr12:3860050
|
A | G | 89 | a0001c0001t0002g0031a0001c0001t0003g0001a0001c0001t0003g0013others(86): Show | 126 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.18+13162T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3860050 | ||||||
| chr12:3860178
|
G | T | 1 | a0001c0001t0006g0226 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.18+13034C>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3860178 | ||||||
| chr12:3860179
|
T | C | 1 | a0001c0001t0007g0208 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.18+13033A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3860179 | ||||||
| chr12:3860494
|
C | T | 1 | a0001c0001t0037g0054 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.18+12718G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3860494 | ||||||
| chr12:3860523
|
C | T | 3 | a0001c0001t0033g0044a0001c0001t0064g0211a0001c0001t0065g0212 | 4 | HG02622.hp1 HG02976.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+12689G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3860523 | ||||||
| chr12:3860563
|
G | T | 40 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(37): Show | 64 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.18+12649C>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3860563 | ||||||
| chr12:3860570
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.18+12642C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3860570 | ||||||
| chr12:3860669
|
A | G | 21 | a0001c0001t0006g0004a0001c0001t0006g0021a0001c0001t0006g0045others(18): Show | 29 | HG00408.hp1 HG00544.hp2 HG02135.hp2 others(26): Show |
intron_variant | MODIFIER | c.18+12543T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3860669 | ||||||
| chr12:3860695
|
T | C | 1 | a0001c0001t0003g0107 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.18+12517A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3860695 | ||||||
| chr12:3860773
|
A | G | 2 | a0001c0001t0034g0136a0001c0001t0034g0137 | 2 | HG02622.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.18+12439T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3860773 | ||||||
| chr12:3860790
|
C | T | 88 | a0001c0001t0002g0031a0001c0001t0003g0001a0001c0001t0003g0013others(85): Show | 125 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.18+12422G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3860790 | ||||||
| chr12:3860841
|
C | T | 165 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(162): Show | 239 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(236): Show |
intron_variant | MODIFIER | c.18+12371G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3860841 | ||||||
| chr12:3860908
|
C | T | 4 | a0001c0001t0006g0214a0001c0001t0006g0215a0001c0001t0006g0296others(1): Show | 4 | HG02135.hp2 NA18983.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+12304G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3860908 | ||||||
| chr12:3861196
|
C | T | 86 | a0001c0001t0003g0001a0001c0001t0003g0013a0001c0001t0003g0014others(83): Show | 122 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.18+12016G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3861196 | ||||||
| chr12:3861379
|
T | C | 1 | a0001c0001t0002g0294 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.18+11833A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3861379 | ||||||
| chr12:3861482
|
A | G | 32 | a0001c0001t0007g0020a0001c0001t0007g0036a0001c0001t0007g0037others(29): Show | 41 | HG01106.hp1 HG01496.hp1 HG01934.hp1 others(38): Show |
intron_variant | MODIFIER | c.18+11730T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3861482 | ||||||
| chr12:3861494
|
T | C | 3 | a0001c0001t0002g0051a0001c0001t0002g0275a0001c0001t0002g0276 | 4 | HG00621.hp2 HG02040.hp2 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.18+11718A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3861494 | ||||||
| chr12:3861606
|
C | T | 1 | a0001c0001t0004g0261 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.18+11606G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3861606 | ||||||
| chr12:3861751
|
G | A | 5 | a0001c0001t0019g0053a0001c0001t0019g0297a0001c0001t0019g0299others(2): Show | 6 | HG01346.hp1 HG02280.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+11461C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3861751 | ||||||
| chr12:3862002
|
T | A | 1 | a0001c0001t0003g0107 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.18+11210A>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3862002 | ||||||
| chr12:3862133
|
A | G | 40 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(37): Show | 64 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.18+11079T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3862133 | ||||||
| chr12:3862147
|
G | T | 32 | a0001c0001t0005g0003a0001c0001t0005g0033a0001c0001t0005g0034others(29): Show | 45 | HG00639.hp2 HG01081.hp1 HG01106.hp2 others(42): Show |
intron_variant | MODIFIER | c.18+11065C>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3862147 | ||||||
| chr12:3862154
|
A | G | 3 | a0001c0001t0002g0051a0001c0001t0002g0275a0001c0001t0002g0276 | 4 | HG00621.hp2 HG02040.hp2 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.18+11058T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3862154 | ||||||
| chr12:3862325
|
C | A | 88 | a0001c0001t0002g0031a0001c0001t0003g0001a0001c0001t0003g0013others(85): Show | 125 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.18+10887G>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3862325 | ||||||
| chr12:3862469
|
A | G | 56 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(53): Show | 86 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.18+10743T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3862469 | ||||||
| chr12:3862469
|
A | T | 1 | a0001c0001t0008g0115 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.18+10743T>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3862469 | ||||||
| chr12:3862569
|
C | G | 1 | a0001c0001t0061g0235 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.18+10643G>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3862569 | ||||||
| chr12:3862594
|
T | C | 29 | a0001c0001t0002g0031a0001c0001t0003g0001a0001c0001t0003g0013others(26): Show | 48 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.18+10618A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3862594 | ||||||
| chr12:3862721
|
G | A | 6 | a0001c0001t0011g0168a0001c0001t0014g0165a0001c0001t0014g0166others(3): Show | 6 | HG01192.hp1 HG01358.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+10491C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3862721 | ||||||
| chr12:3862804
|
A | G | 1 | a0001c0001t0028g0035 | 2 | HG01261.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.18+10408T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3862804 | ||||||
| chr12:3862928
|
C | A | 191 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(188): Show | 279 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.18+10284G>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3862928 | ||||||
| chr12:3862940
|
T | C | 31 | a0001c0001t0002g0031a0001c0001t0003g0001a0001c0001t0003g0013others(28): Show | 50 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.18+10272A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3862940 | ||||||
| chr12:3863010
|
T | C | 6 | a0001c0001t0017g0010a0001c0001t0023g0161a0001c0001t0023g0162others(3): Show | 9 | HG00323.hp1 HG00642.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.18+10202A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3863010 | ||||||
| chr12:3863060
|
G | GT | 2 | a0001c0001t0002g0050a0001c0001t0002g0274 | 3 | NA18952.hp1 NA18966.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.18+10151dupA | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3863060 | ||||||
| chr12:3863096
|
C | G | 28 | a0001c0001t0002g0031a0001c0001t0003g0001a0001c0001t0003g0013others(25): Show | 47 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.18+10116G>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3863096 | ||||||
| chr12:3863152
|
G | C | 1 | a0001c0001t0007g0208 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.18+10060C>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3863152 | ||||||
| chr12:3863156
|
A | G | 29 | a0001c0001t0002g0031a0001c0001t0003g0001a0001c0001t0003g0013others(26): Show | 48 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.18+10056T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3863156 | ||||||
| chr12:3863192
|
T | C | 6 | a0001c0001t0002g0043a0001c0001t0015g0012a0001c0001t0015g0030others(3): Show | 12 | HG01952.hp2 HG02258.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.18+10020A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3863192 | ||||||
| chr12:3863639
|
G | A | 1 | a0001c0001t0005g0180 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.18+9573C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3863639 | ||||||
| chr12:3863644
|
C | A | 1 | a0001c0001t0006g0226 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.18+9568G>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3863644 | ||||||
| chr12:3863684
|
G | A | 59 | a0001c0001t0006g0004a0001c0001t0006g0021a0001c0001t0006g0045others(56): Show | 77 | HG00408.hp1 HG00544.hp2 HG01106.hp1 others(74): Show |
intron_variant | MODIFIER | c.18+9528C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3863684 | ||||||
| chr12:3863783
|
G | A | 5 | a0001c0001t0019g0053a0001c0001t0019g0297a0001c0001t0019g0299others(2): Show | 6 | HG01346.hp1 HG02280.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+9429C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3863783 | ||||||
| chr12:3863956
|
C | T | 37 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(34): Show | 61 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.18+9256G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3863956 | ||||||
| chr12:3864007
|
GGACA | G | 27 | a0001c0001t0003g0001a0001c0001t0003g0013a0001c0001t0003g0014others(24): Show | 45 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.18+9201_18+9204del others(4): Show |
PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3864007 | ||||||
| chr12:3864040
|
A | G | 111 | a0001c0001t0002g0043a0001c0001t0003g0001a0001c0001t0003g0013others(108): Show | 159 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.18+9172T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3864040 | ||||||
| chr12:3864706
|
A | C | 1 | a0001c0001t0069g0147 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.18+8506T>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3864706 | ||||||
| chr12:3864715
|
T | C | 2 | a0001c0001t0005g0181a0001c0001t0005g0182 | 2 | NA18957.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.18+8497A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3864715 | ||||||
| chr12:3864827
|
T | C | 1 | a0001c0001t0014g0183 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.18+8385A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3864827 | ||||||
| chr12:3864865
|
T | C | 2 | a0001c0001t0028g0035a0001c0001t0071g0230 | 3 | HG01261.hp2 HG01358.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.18+8347A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3864865 | ||||||
| chr12:3865061
|
T | C | 3 | a0001c0001t0005g0209a0001c0001t0005g0229a0001c0001t0042g0058 | 3 | HG02109.hp1 HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.18+8151A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3865061 | ||||||
| chr12:3865199
|
A | G | 1 | a0001c0001t0003g0087 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.18+8013T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3865199 | ||||||
| chr12:3865239
|
A | T | 1 | a0001c0001t0004g0046 | 2 | HG02040.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.18+7973T>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3865239 | ||||||
| chr12:3865289
|
G | A | 40 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(37): Show | 64 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.18+7923C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3865289 | ||||||
| chr12:3865319
|
C | T | 1 | a0001c0001t0003g0029 | 2 | HG02004.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.18+7893G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3865319 | ||||||
| chr12:3865418
|
T | C | 5 | a0001c0001t0019g0053a0001c0001t0019g0297a0001c0001t0019g0299others(2): Show | 6 | HG01346.hp1 HG02280.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+7794A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3865418 | ||||||
| chr12:3865482
|
T | C | 29 | a0001c0001t0002g0031a0001c0001t0003g0001a0001c0001t0003g0013others(26): Show | 48 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.18+7730A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3865482 | ||||||
| chr12:3865889
|
C | CT | 167 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(164): Show | 247 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(244): Show |
intron_variant | MODIFIER | c.18+7322dupA | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3865889 | ||||||
| chr12:3865995
|
C | T | 1 | a0001c0001t0043g0085 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.18+7217G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3865995 | ||||||
| chr12:3866100
|
T | A | 40 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(37): Show | 64 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.18+7112A>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3866100 | ||||||
| chr12:3866218
|
C | T | 5 | a0001c0001t0019g0053a0001c0001t0019g0297a0001c0001t0019g0299others(2): Show | 6 | HG01346.hp1 HG02280.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+6994G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3866218 | ||||||
| chr12:3866313
|
C | T | 1 | a0001c0001t0005g0040 | 2 | HG02280.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.18+6899G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3866313 | ||||||
| chr12:3866519
|
C | T | 39 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(36): Show | 63 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.18+6693G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3866519 | ||||||
| chr12:3866659
|
AT | A | 108 | a0001c0001t0003g0001a0001c0001t0003g0013a0001c0001t0003g0014others(105): Show | 153 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(150): Show |
intron_variant | MODIFIER | c.18+6552delA | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3866659 | ||||||
| chr12:3866757
|
T | G | 32 | a0001c0001t0007g0020a0001c0001t0007g0036a0001c0001t0007g0037others(29): Show | 41 | HG01106.hp1 HG01496.hp1 HG01934.hp1 others(38): Show |
intron_variant | MODIFIER | c.18+6455A>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3866757 | ||||||
| chr12:3866855
|
ATATATTA others(6): Show |
A | 129 | a0001c0001t0002g0273a0001c0001t0003g0001a0001c0001t0003g0013others(126): Show | 180 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.18+6344_18+6356del others(13): Show |
PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3866855 | ||||||
| chr12:3867334
|
G | A | 1 | a0001c0001t0006g0227 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.18+5878C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3867334 | ||||||
| chr12:3867418
|
T | A | 1 | a0001c0001t0004g0261 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.18+5794A>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3867418 | ||||||
| chr12:3867534
|
G | A | 7 | a0001c0001t0005g0040a0001c0001t0005g0041a0001c0001t0005g0042others(4): Show | 10 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.18+5678C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3867534 | ||||||
| chr12:3867543
|
C | T | 1 | a0001c0001t0004g0234 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.18+5669G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3867543 | ||||||
| chr12:3867773
|
A | T | 1 | a0001c0001t0001g0114 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.18+5439T>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3867773 | ||||||
| chr12:3867842
|
C | T | 3 | a0001c0001t0069g0147a0001c0001t0070g0139a0001c0001t0071g0230 | 3 | HG02615.hp2 HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.18+5370G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3867842 | ||||||
| chr12:3867907
|
A | G | 18 | a0001c0001t0002g0273a0001c0001t0011g0048a0001c0001t0011g0049others(15): Show | 24 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(21): Show |
intron_variant | MODIFIER | c.18+5305T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3867907 | ||||||
| chr12:3867965
|
G | A | 1 | a0001c0001t0071g0230 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.18+5247C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3867965 | ||||||
| chr12:3868098
|
C | T | 1 | a0001c0001t0069g0147 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.18+5114G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3868098 | ||||||
| chr12:3868199
|
G | A | 4 | a0001c0001t0005g0040a0001c0001t0005g0041a0001c0001t0005g0042others(1): Show | 7 | HG01884.hp2 HG02257.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.18+5013C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3868199 | ||||||
| chr12:3868523
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.18+4689G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3868523 | ||||||
| chr12:3868546
|
C | T | 27 | a0001c0001t0003g0001a0001c0001t0003g0013a0001c0001t0003g0014others(24): Show | 45 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.18+4666G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3868546 | ||||||
| chr12:3868610
|
T | C | 2 | a0001c0001t0002g0043a0001c0001t0015g0012 | 6 | HG01952.hp2 HG02258.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.18+4602A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3868610 | ||||||
| chr12:3868615
|
C | T | 1 | a0001c0001t0004g0233 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.18+4597G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3868615 | ||||||
| chr12:3868626
|
T | C | 1 | a0001c0001t0050g0140 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.18+4586A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3868626 | ||||||
| chr12:3868792
|
T | C | 24 | a0001c0001t0003g0100a0001c0001t0008g0295a0001c0001t0010g0027others(21): Show | 26 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.18+4420A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3868792 | ||||||
| chr12:3868847
|
A | G | 2 | a0001c0001t0002g0022a0001c0001t0004g0232 | 4 | HG00738.hp2 HG01074.hp1 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+4365T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3868847 | ||||||
| chr12:3868943
|
A | G | 1 | a0001c0001t0004g0231 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.18+4269T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3868943 | ||||||
| chr12:3869016
|
AC | A | 3 | a0001c0001t0033g0044a0001c0001t0064g0211a0001c0001t0065g0212 | 4 | HG02622.hp1 HG02976.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+4195delG | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3869016 | ||||||
| chr12:3869090
|
T | G | 5 | a0001c0001t0019g0053a0001c0001t0019g0297a0001c0001t0019g0299others(2): Show | 6 | HG01346.hp1 HG02280.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+4122A>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3869090 | ||||||
| chr12:3869195
|
G | A | 1 | a0001c0001t0012g0076 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.18+4017C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3869195 | ||||||
| chr12:3869284
|
C | T | 1 | a0001c0001t0001g0112 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.18+3928G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3869284 | ||||||
| chr12:3869495
|
C | A | 40 | a0001c0001t0002g0022a0001c0001t0002g0024a0001c0001t0002g0239others(37): Show | 52 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.18+3717G>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3869495 | ||||||
| chr12:3869505
|
T | C | 1 | a0001c0001t0003g0101 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.18+3707A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3869505 | ||||||
| chr12:3870069
|
T | G | 21 | a0001c0001t0006g0004a0001c0001t0006g0021a0001c0001t0006g0045others(18): Show | 29 | HG00408.hp1 HG00544.hp2 HG02135.hp2 others(26): Show |
intron_variant | MODIFIER | c.18+3143A>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3870069 | ||||||
| chr12:3870143
|
A | G | 2 | a0001c0001t0005g0143a0001c0001t0005g0144 | 2 | HG03239.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.18+3069T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3870143 | ||||||
| chr12:3870258
|
T | C | 1 | a0001c0001t0012g0076 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.18+2954A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3870258 | ||||||
| chr12:3870292
|
G | A | 1 | a0001c0001t0003g0102 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.18+2920C>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3870292 | ||||||
| chr12:3870381
|
G | C | 6 | a0001c0001t0003g0015a0001c0001t0003g0105a0001c0001t0003g0106others(3): Show | 8 | HG02132.hp1 NA18959.hp2 NA18968.hp2 others(5): Show |
intron_variant | MODIFIER | c.18+2831C>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3870381 | ||||||
| chr12:3870434
|
T | C | 1 | a0001c0001t0040g0077 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.18+2778A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3870434 | ||||||
| chr12:3870687
|
T | C | 5 | a0001c0001t0019g0053a0001c0001t0019g0297a0001c0001t0019g0299others(2): Show | 6 | HG01346.hp1 HG02280.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+2525A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3870687 | ||||||
| chr12:3870923
|
T | G | 1 | a0001c0001t0005g0228 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.18+2289A>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3870923 | ||||||
| chr12:3871359
|
T | C | 1 | a0001c0001t0005g0229 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.18+1853A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3871359 | ||||||
| chr12:3871592
|
A | G | 1 | a0001c0001t0010g0059 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.18+1620T>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3871592 | ||||||
| chr12:3871745
|
T | C | 1 | a0001c0001t0071g0230 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.18+1467A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3871745 | ||||||
| chr12:3871790
|
C | T | 41 | a0001c0001t0002g0022a0001c0001t0002g0024a0001c0001t0002g0138others(38): Show | 53 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.18+1422G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3871790 | ||||||
| chr12:3871856
|
C | G | 1 | a0001c0001t0002g0138 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.18+1356G>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3871856 | ||||||
| chr12:3871975
|
GATCCCTC others(8): Show |
G | 1 | a0001c0001t0006g0142 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.18+1222_18+1236del others(15): Show |
PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3871975 | ||||||
| chr12:3872090
|
C | T | 1 | a0001c0001t0062g0141 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.18+1122G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3872090 | ||||||
| chr12:3872115
|
A | T | 191 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(188): Show | 279 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.18+1097T>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3872115 | ||||||
| chr12:3872194
|
C | A | 1 | a0001c0001t0050g0140 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.18+1018G>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3872194 | ||||||
| chr12:3872293
|
T | C | 1 | a0001c0001t0001g0019 | 3 | HG00673.hp1 NA18949.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.18+919A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3872293 | ||||||
| chr12:3872435
|
C | T | 1 | a0001c0001t0050g0140 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.18+777G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3872435 | ||||||
| chr12:3872542
|
C | G | 1 | a0001c0001t0001g0111 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.18+670G>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3872542 | ||||||
| chr12:3872589
|
A | T | 1 | a0001c0001t0070g0139 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.18+623T>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3872589 | ||||||
| chr12:3872691
|
A | T | 2 | a0001c0001t0003g0013a0001c0001t0003g0029 | 5 | HG00423.hp1 HG00597.hp1 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+521T>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3872691 | ||||||
| chr12:3872821
|
G | T | 38 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0017others(35): Show | 62 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.18+391C>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3872821 | ||||||
| chr12:3872848
|
C | G | 3 | a0001c0001t0008g0108a0001c0001t0008g0109a0001c0001t0008g0110 | 3 | HG02559.hp2 HG02895.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.18+364G>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3872848 | ||||||
| chr12:3872917
|
C | T | 5 | a0001c0001t0019g0053a0001c0001t0019g0297a0001c0001t0019g0299others(2): Show | 6 | HG01346.hp1 HG02280.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+295G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3872917 | ||||||
| chr12:3872934
|
C | G | 1 | a0001c0001t0012g0057 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.18+278G>C | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3872934 | ||||||
| chr12:3873055
|
G | T | 26 | a0001c0001t0003g0001a0001c0001t0003g0013a0001c0001t0003g0014others(23): Show | 44 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.18+157C>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3873055 |