Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1014 | 415 | 92 | 68 | 199 | 10 | 44 | PARP11_chr12_3803861_3878399 | PARP11 | ATGTG others(1009): Show |
chr12 | 3803861 | 3878399 | ||
| a0001c0002 | 0/0 | 1014 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | ATGTG others(1009): Show |
chr12 | 3803861 | 3878399 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4427 | 45 | 9 | 0 | 33 | 0 | 3 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4422): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0002 | 0/0 | 4445 | 43 | 4 | 8 | 27 | 0 | 4 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4440): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0003 | 0/0 | 4445 | 40 | 1 | 5 | 34 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4440): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0004 | 1/0 | 4449 | 37 | 2 | 12 | 13 | 3 | 6 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4444): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0005 | 0/0 | 4455 | 36 | 11 | 9 | 8 | 2 | 6 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4450): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0006 | 0/0 | 4458 | 25 | 2 | 0 | 18 | 0 | 5 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4453): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0007 | 0/0 | 4465 | 18 | 0 | 0 | 18 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4460): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0008 | 0/0 | 4441 | 16 | 13 | 1 | 0 | 0 | 2 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4436): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0009 | 0/0 | 4447 | 12 | 12 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4442): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0010 | 0/0 | 4441 | 11 | 2 | 1 | 3 | 2 | 3 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4436): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0011 | 0/0 | 4452 | 9 | 2 | 0 | 3 | 1 | 3 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4447): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0012 | 0/0 | 4445 | 6 | 0 | 5 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4440): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0013 | 0/0 | 4459 | 6 | 1 | 5 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4454): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0014 | 0/0 | 4448 | 6 | 3 | 2 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4443): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0015 | 0/0 | 4446 | 6 | 5 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4441): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0016 | 0/0 | 4452 | 6 | 0 | 0 | 6 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4447): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0017 | 0/0 | 4439 | 4 | 0 | 2 | 0 | 0 | 2 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4434): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0018 | 0/0 | 4469 | 4 | 0 | 0 | 4 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4464): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0019 | 0/0 | 4458 | 4 | 3 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4453): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0020 | 0/0 | 4449 | 3 | 0 | 2 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4444): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0021 | 0/0 | 4450 | 3 | 0 | 2 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4445): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0022 | 0/0 | 4465 | 3 | 0 | 0 | 3 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4460): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0023 | 0/0 | 4435 | 3 | 0 | 0 | 2 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4430): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0024 | 0/0 | 4445 | 2 | 0 | 1 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4440): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0025 | 0/0 | 4441 | 2 | 0 | 2 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4436): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0026 | 0/0 | 4428 | 2 | 0 | 0 | 2 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4423): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0027 | 0/0 | 4456 | 2 | 0 | 1 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4451): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0028 | 0/0 | 4458 | 2 | 0 | 2 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4453): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0029 | 0/0 | 4455 | 2 | 0 | 2 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4450): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0030 | 0/0 | 4432 | 2 | 0 | 1 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4427): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0031 | 0/0 | 4473 | 2 | 0 | 0 | 2 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4468): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0032 | 0/0 | 4461 | 2 | 0 | 0 | 2 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4456): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0033 | 0/0 | 4467 | 2 | 2 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4462): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0034 | 0/0 | 4461 | 2 | 2 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4456): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0035 | 0/0 | 4445 | 2 | 0 | 0 | 2 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4440): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0036 | 0/0 | 4445 | 2 | 0 | 0 | 2 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4440): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0037 | 0/0 | 4454 | 2 | 2 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4449): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0038 | 0/0 | 4443 | 1 | 0 | 0 | 0 | 1 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4438): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0039 | 0/0 | 4431 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4426): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0040 | 0/0 | 4426 | 1 | 0 | 0 | 0 | 1 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4421): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0041 | 0/0 | 4441 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4436): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0042 | 0/0 | 4452 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4447): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0043 | 0/0 | 4455 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4450): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0044 | 0/0 | 4453 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4448): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0045 | 0/0 | 4446 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4441): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0046 | 0/0 | 4466 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4461): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0047 | 0/0 | 4467 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4462): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0048 | 0/0 | 4449 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4444): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0049 | 0/0 | 4469 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4464): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0050 | 0/0 | 4457 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4452): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0051 | 0/0 | 4449 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4444): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0052 | 0/0 | 4450 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4445): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0053 | 0/0 | 4439 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4434): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0054 | 0/0 | 4428 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4423): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0055 | 0/0 | 4456 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4451): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0056 | 0/0 | 4452 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4447): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0057 | 0/0 | 4453 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4448): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0058 | 0/1 | 4453 | 1 | 0 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4448): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0059 | 0/0 | 4453 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4448): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0060 | 0/0 | 4452 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4447): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0061 | 0/0 | 4449 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4444): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0062 | 0/0 | 4449 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4444): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0063 | 0/0 | 4465 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4460): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0064 | 0/0 | 4461 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4456): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0065 | 0/0 | 4471 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4466): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0066 | 0/0 | 4463 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4458): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0067 | 0/0 | 4462 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4457): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0068 | 0/0 | 4442 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4437): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0069 | 0/0 | 4441 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4436): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0070 | 0/0 | 4455 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4450): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0071 | 0/0 | 4461 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4456): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0072 | 0/0 | 4461 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4456): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0073 | 0/0 | 4447 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4442): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0074 | 0/0 | 4455 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4450): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0075 | 0/0 | 4461 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4456): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0076 | 0/0 | 4456 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4451): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0077 | 0/0 | 4445 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4440): Show |
chr12 | 3803861 | 3878399 |
| a0001c0001t0078 | 0/0 | 4445 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4440): Show |
chr12 | 3803861 | 3878399 |
| a0001c0002t0003 | 0/0 | 4445 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | GGTCT others(4440): Show |
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 |
| a0001c0001t0001g0134 | 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 |
| a0001c0001t0004g0290 | 1/0 | 1 | 0 | 0 | 0 | 0 | 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 |
| 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 |
| a0001c0001t0022g0186 | 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 |
| a0001c0001t0029g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0030g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0030g0135 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0036g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0036g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0037g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0037g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0038g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0039g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0040g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0041g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0042g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0043g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0044g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0045g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0046g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0047g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0048g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0049g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0050g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0051g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0052g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0053g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0054g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0055g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0056g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0057g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0058g0264 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0059g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0060g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0061g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0062g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0063g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0064g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0065g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0066g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0067g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0068g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0069g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0070g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0071g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0072g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0073g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0074g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0075g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0076g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| a0001c0001t0077g0284 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| 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 | t0038 | 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 | t0068 | 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 | t0044 | 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 | t0060 | 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 | t0062 | 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 | t0048 | 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 | t0030 | g0135 | 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 | t0029 | 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 | t0073 | g0154 | AFR | ACB | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01891 | hp2 | a0001 | c0001 | t0052 | g0167 | AFR | ACB | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01934 | hp1 | a0001 | c0001 | t0029 | g0038 | AMR | PEL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG01934 | hp2 | a0001 | c0001 | t0061 | 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 | t0036 | 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 | t0075 | 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 | t0051 | 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 | t0050 | g0189 | 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 | t0049 | g0187 | 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 | g0188 | 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 | t0037 | 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 | t0069 | g0156 | AFR | ACB | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02523 | hp1 | a0001 | c0001 | t0055 | 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 | t0039 | 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 | t0070 | 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 | t0042 | 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 | t0030 | g0121 | SAS | PJL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG02735 | hp2 | a0001 | c0001 | t0041 | 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 | t0072 | 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 | t0043 | 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 | t0066 | g0212 | AFR | ESN | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG03017 | hp1 | a0001 | c0001 | t0056 | 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 | t0065 | 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 | t0064 | g0148 | AFR | MSL | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| HG03225 | hp1 | a0001 | c0001 | t0074 | 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 | t0071 | 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 | t0047 | 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 | t0076 | 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 | g0186 | 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 | g0185 | 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 | t0046 | 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 | t0067 | 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 | t0036 | 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 | t0054 | g0120 | 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 | t0053 | 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 | g0134 | 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 | t0063 | 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 | t0045 | 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 | t0037 | 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 | t0040 | 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 | t0057 | 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 | t0077 | 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 | t0059 | 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 | a0001 | c0001 | t0058 | g0264 | REF | REF | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0290 | REF | REF | PARP11_chr12_3803861_3878399 | PARP11 | chr12 | 3803861 | 3878399 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:3808872 | G | A | 5 | a0001c0001t0006 a0001c0001t0047 a0001c0001t0060 others(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 | a0001c0001t0072 | 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 | 38 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(35): Show |
202 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(199): 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 | a0001c0001t0005 a0001c0001t0027 a0001c0001t0043 others(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 | a0001c0001t0005 a0001c0001t0027 a0001c0001t0043 others(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 | a0001c0001t0074 | 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 | 60 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(57): Show |
283 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(280): 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 | a0001c0001t0005 a0001c0001t0027 a0001c0001t0043 others(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 | a0001c0001t0007 a0001c0001t0013 a0001c0001t0018 others(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 | ||||||
| chr12:3809586 | G | GT | 2 | a0001c0001t0019 a0001c0001t0037 |
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 | 29 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0006 others(26): Show |
153 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(150): 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 | a0001c0001t0051 | 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 | 5 | a0001c0001t0003 a0001c0001t0035 a0001c0001t0036 others(2): 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 | a0001c0001t0063 | 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 | a0001c0001t0062 | 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 | a0001c0001t0033 a0001c0001t0065 a0001c0001t0066 |
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 | a0001c0001t0056 | 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 | a0001c0001t0005 a0001c0001t0027 a0001c0001t0043 others(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 | a0001c0001t0039 | 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 | a0001c0001t0061 | 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 | a0001c0001t0003 a0001c0001t0035 a0001c0002t0003 |
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 | a0001c0001t0003 a0001c0002t0003 |
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 | a0001c0001t0006 a0001c0001t0011 a0001c0001t0016 others(7): Show |
48 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(45): 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 | a0001c0001t0019 a0001c0001t0050 a0001c0001t0052 others(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 | a0001c0001t0029 a0001c0001t0032 a0001c0001t0033 others(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 | a0001c0001t0007 a0001c0001t0013 a0001c0001t0022 others(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 | a0001c0001t0018 a0001c0001t0049 |
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 | a0001c0001t0003 a0001c0001t0035 a0001c0002t0003 |
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 | a0001c0001t0002 a0001c0001t0012 a0001c0001t0015 others(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 | a0001c0001t0008 a0001c0001t0009 a0001c0001t0010 others(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 | a0001c0001t0005 a0001c0001t0027 a0001c0001t0039 others(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 | a0001c0001t0001 a0001c0001t0026 a0001c0001t0030 others(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 | a0001c0001t0040 | 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 | a0001c0001t0036 | 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 | a0001c0001t0033 a0001c0001t0065 a0001c0001t0066 |
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 | a0001c0001t0001 a0001c0001t0013 a0001c0001t0026 others(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 | a0001c0001t0030 | 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 | a0001c0001t0007 a0001c0001t0015 a0001c0001t0018 others(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 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0009 others(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 | a0001c0001t0034 a0001c0001t0075 |
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 | a0001c0001t0017 a0001c0001t0023 a0001c0001t0038 others(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 | 5 | a0001c0001t0003 a0001c0001t0035 a0001c0001t0036 others(2): 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 | a0001c0001t0051 | 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 | a0001c0001t0009 a0001c0001t0017 a0001c0001t0023 others(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 | a0001c0001t0073 | 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 | a0001c0001t0005 a0001c0001t0027 a0001c0001t0043 others(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 | a0001c0001t0022 a0001c0001t0049 a0001c0001t0050 |
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 | a0001c0001t0016 a0001c0001t0076 |
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 | a0001c0001t0077 | 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 | 5 | a0001c0001t0003 a0001c0001t0035 a0001c0001t0036 others(2): 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 | a0001c0001t0048 | 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 | a0001c0001t0041 | 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 | a0001c0001t0021 a0001c0001t0026 a0001c0001t0027 others(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 | a0001c0001t0010 a0001c0001t0012 a0001c0001t0020 others(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 | a0001c0001t0017 a0001c0001t0038 a0001c0001t0039 |
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 | a0001c0001t0019 a0001c0001t0037 |
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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:3812581 | AGAG | A | 7 | a0001c0001t0011g0168 a0001c0001t0014g0118 a0001c0001t0014g0165 others(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 | a0001c0001t0007g0020 a0001c0001t0007g0036 a0001c0001t0007g0037 others(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 | a0001c0001t0006g0004 a0001c0001t0006g0021 a0001c0001t0006g0045 others(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 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0030g0135 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(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 | a0001c0001t0064g0148 | 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 | 78 | a0001c0001t0003g0001 a0001c0001t0003g0013 a0001c0001t0003g0014 others(75): Show |
112 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(109): 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 | a0001c0001t0003g0001 a0001c0001t0003g0013 a0001c0001t0003g0014 others(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 | 78 | a0001c0001t0003g0001 a0001c0001t0003g0013 a0001c0001t0003g0014 others(75): Show |
112 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(109): 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 | a0001c0001t0009g0006 a0001c0001t0009g0032 a0001c0001t0009g0153 others(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 | a0001c0001t0006g0004 a0001c0001t0006g0021 a0001c0001t0006g0045 others(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 | a0001c0001t0006g0004 a0001c0001t0006g0021 a0001c0001t0006g0045 others(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 | a0001c0001t0005g0003 a0001c0001t0005g0033 a0001c0001t0005g0034 others(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 | a0001c0001t0006g0004 a0001c0001t0006g0021 a0001c0001t0006g0045 others(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 | 196 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(193): Show |
284 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(281): 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 | a0001c0001t0009g0006 a0001c0001t0009g0032 a0001c0001t0009g0153 others(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 | 77 | a0001c0001t0002g0273 a0001c0001t0003g0001 a0001c0001t0003g0013 others(74): Show |
114 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(111): 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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(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 | a0001c0001t0064g0148 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(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 | a0001c0001t0005g0003 a0001c0001t0005g0033 a0001c0001t0005g0034 others(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 | a0001c0001t0009g0006 a0001c0001t0009g0032 a0001c0001t0009g0153 others(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 | a0001c0001t0009g0006 a0001c0001t0009g0158 a0001c0001t0009g0159 others(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 | a0001c0001t0034g0136 a0001c0001t0034g0137 |
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 | a0001c0001t0009g0006 a0001c0001t0009g0032 a0001c0001t0009g0153 others(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 | a0001c0001t0070g0147 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(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 | a0001c0001t0019g0053 a0001c0001t0019g0297 a0001c0001t0019g0299 others(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 | 162 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(159): Show |
236 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.549-3003dupT | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 6/7 | chr12 | 3817190 | |||||||
| chr12:3817190 | C | CAA | 32 | a0001c0001t0005g0003 a0001c0001t0005g0033 a0001c0001t0005g0034 others(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 | a0001c0001t0015g0012 a0001c0001t0015g0030 a0001c0001t0033g0044 others(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 | a0001c0001t0072g0230 | 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 | a0001c0001t0019g0053 a0001c0001t0019g0297 a0001c0001t0019g0299 others(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 | a0001c0001t0033g0044 a0001c0001t0065g0211 a0001c0001t0066g0212 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(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 | a0001c0001t0005g0003 a0001c0001t0005g0033 a0001c0001t0005g0034 others(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 | a0001c0001t0019g0297 a0001c0001t0019g0299 a0001c0001t0037g0298 others(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 | a0001c0001t0033g0044 a0001c0001t0065g0211 a0001c0001t0066g0212 |
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 | a0001c0001t0005g0177 a0001c0001t0005g0178 |
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 | a0001c0001t0039g0055 | 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 | a0001c0001t0003g0001 a0001c0001t0003g0013 a0001c0001t0003g0014 others(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 | 269 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(266): Show |
375 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(372): 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 | a0001c0001t0070g0147 a0001c0001t0071g0139 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(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 | a0001c0001t0019g0053 a0001c0001t0019g0297 a0001c0001t0019g0299 others(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 | a0001c0001t0009g0006 a0001c0001t0009g0032 a0001c0001t0009g0153 others(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 | 22 | a0001c0001t0011g0048 a0001c0001t0011g0049 a0001c0001t0011g0168 others(19): Show |
28 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(25): 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 | a0001c0001t0064g0148 | 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 | a0001c0001t0071g0139 | 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 | a0001c0001t0003g0001 a0001c0001t0003g0013 a0001c0001t0003g0014 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(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 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0030g0135 |
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 | a0001c0001t0005g0040 a0001c0001t0005g0041 a0001c0001t0005g0042 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(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 | a0001c0001t0002g0116 a0001c0001t0008g0016 a0001c0001t0008g0018 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(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 | a0001c0001t0003g0001 a0001c0001t0003g0013 a0001c0001t0003g0014 others(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 | a0001c0001t0070g0147 a0001c0001t0071g0139 |
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 | a0001c0001t0005g0171 a0001c0001t0055g0263 |
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 | a0001c0001t0019g0053 a0001c0001t0019g0297 a0001c0001t0019g0299 others(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 | a0001c0001t0002g0248 a0001c0001t0002g0276 a0001c0001t0002g0278 others(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 | 114 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(111): Show |
164 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(161): 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 | a0001c0001t0003g0001 a0001c0001t0003g0013 a0001c0001t0003g0014 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(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 | 173 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(170): Show |
252 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(249): 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 | a0001c0001t0063g0141 | 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 | a0001c0001t0009g0153 a0001c0001t0069g0156 |
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 | 16 | a0001c0001t0002g0273 a0001c0001t0011g0048 a0001c0001t0011g0049 others(13): Show |
22 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(19): 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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(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 | a0001c0001t0051g0140 | 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 | a0001c0001t0002g0022 a0001c0001t0004g0232 |
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 | 171 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(168): Show |
246 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(243): 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 | a0001c0001t0066g0212 | 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 | a0001c0001t0005g0003 a0001c0001t0005g0033 a0001c0001t0005g0034 others(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 | a0001c0001t0019g0053 a0001c0001t0019g0297 a0001c0001t0019g0299 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(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 | a0001c0001t0006g0221 a0001c0001t0060g0220 |
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 | a0001c0001t0051g0140 | 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 | a0001c0001t0002g0273 a0001c0001t0002g0293 a0001c0001t0003g0106 others(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 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(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 | a0001c0001t0064g0148 | 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 | a0001c0001t0001g0122 a0001c0001t0001g0132 |
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 | a0001c0001t0003g0001 a0001c0001t0003g0013 a0001c0001t0003g0014 others(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 | a0001c0001t0019g0053 a0001c0001t0019g0297 a0001c0001t0019g0299 others(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 | a0001c0001t0019g0053 a0001c0001t0019g0297 a0001c0001t0019g0299 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(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 | a0001c0001t0004g0160 a0001c0001t0004g0244 |
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 | a0001c0001t0019g0053 a0001c0001t0019g0297 a0001c0001t0019g0299 others(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 | a0001c0001t0008g0108 a0001c0001t0008g0110 |
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 | a0001c0001t0007g0020 a0001c0001t0007g0036 a0001c0001t0007g0037 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(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 | a0001c0001t0019g0053 a0001c0001t0019g0297 a0001c0001t0019g0299 others(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 | a0001c0001t0064g0148 | 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 | a0001c0001t0006g0226 a0001c0001t0011g0265 a0001c0001t0028g0035 |
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 | a0001c0001t0002g0116 a0001c0001t0008g0016 a0001c0001t0008g0018 others(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 | a0001c0001t0015g0012 a0001c0001t0015g0030 |
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 | a0001c0001t0034g0136 a0001c0001t0034g0137 |
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 | a0001c0001t0001g0151 a0001c0001t0001g0152 |
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 | a0001c0001t0002g0116 a0001c0001t0008g0016 a0001c0001t0008g0018 others(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 | a0001c0001t0005g0003 a0001c0001t0005g0033 a0001c0001t0005g0034 others(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 | a0001c0001t0006g0004 a0001c0001t0006g0021 a0001c0001t0006g0045 others(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 | a0001c0001t0034g0136 a0001c0001t0034g0137 |
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 | a0001c0001t0012g0026 a0001c0001t0012g0057 a0001c0001t0012g0061 others(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 | 83 | a0001c0001t0002g0273 a0001c0001t0003g0001 a0001c0001t0003g0013 others(80): Show |
122 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.269-1137A>G | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 3/7 | chr12 | 3827370 | |||||||
| chr12:3827466 | T | G | 22 | a0001c0001t0002g0273 a0001c0001t0011g0048 a0001c0001t0011g0049 others(19): Show |
28 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(25): 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 | 83 | a0001c0001t0002g0273 a0001c0001t0003g0001 a0001c0001t0003g0013 others(80): Show |
122 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(119): 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 | a0001c0001t0007g0020 a0001c0001t0007g0036 a0001c0001t0007g0037 others(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 | a0001c0001t0053g0291 | 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 | a0001c0001t0006g0004 a0001c0001t0006g0021 a0001c0001t0006g0045 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(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 | a0001c0001t0071g0139 | 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 | 18 | a0001c0001t0002g0273 a0001c0001t0002g0276 a0001c0001t0002g0278 others(15): Show |
24 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(21): Show |
intron_variant | MODIFIER | c.268+365dupT | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 3/7 | chr12 | 3828544 | |||||||
| chr12:3828544 | C | CAA | 8 | a0001c0001t0011g0168 a0001c0001t0014g0165 a0001c0001t0014g0166 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(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 | a0001c0001t0007g0199 a0001c0001t0022g0185 a0001c0001t0022g0186 others(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 | a0001c0001t0002g0116 a0001c0001t0008g0016 a0001c0001t0008g0018 others(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 | a0001c0001t0003g0001 a0001c0001t0003g0013 a0001c0001t0003g0014 others(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 | a0001c0001t0015g0012 a0001c0001t0015g0030 a0001c0001t0033g0044 others(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 | a0001c0001t0002g0289 a0001c0001t0077g0284 |
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 | a0001c0001t0002g0050 a0001c0001t0002g0274 a0001c0001t0002g0292 others(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 | a0001c0001t0061g0241 | 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 | a0001c0001t0022g0188 a0001c0001t0050g0189 |
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 | a0001c0001t0004g0251 a0001c0001t0021g0083 a0001c0001t0062g0235 |
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 | a0001c0001t0033g0044 a0001c0001t0065g0211 a0001c0001t0066g0212 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(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 | a0001c0001t0005g0003 a0001c0001t0005g0033 a0001c0001t0005g0034 others(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 | 178 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(175): Show |
258 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(255): 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 | a0001c0001t0015g0012 a0001c0001t0015g0030 |
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 | a0001c0001t0007g0020 a0001c0001t0007g0036 a0001c0001t0007g0037 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(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 | a0001c0001t0071g0139 | 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 | a0001c0001t0005g0177 a0001c0001t0005g0178 |
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 | a0001c0001t0070g0147 a0001c0001t0071g0139 a0001c0001t0072g0230 |
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 | a0001c0001t0007g0020 a0001c0001t0007g0036 a0001c0001t0007g0037 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(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 | a0001c0001t0002g0116 a0001c0001t0008g0016 a0001c0001t0008g0018 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(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 | a0001c0001t0019g0053 a0001c0001t0019g0297 a0001c0001t0019g0299 others(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 | a0001c0001t0009g0006 a0001c0001t0009g0158 a0001c0001t0073g0154 |
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 | a0001c0001t0071g0139 | 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 | a0001c0001t0011g0168 a0001c0001t0014g0165 a0001c0001t0014g0166 others(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 | a0001c0001t0017g0010 a0001c0001t0038g0054 a0001c0001t0039g0055 |
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 | a0001c0001t0003g0001 a0001c0001t0003g0013 a0001c0001t0003g0014 others(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 | 1 | a0001c0001t0011g0049 | 2 | HG00323.hp2 HG06807.hp2 |
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 | a0001c0001t0064g0148 | 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 | a0001c0001t0064g0148 | 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 | a0001c0001t0007g0020 a0001c0001t0007g0036 a0001c0001t0007g0037 others(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 | a0001c0001t0001g0151 a0001c0001t0001g0152 |
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 | a0001c0001t0002g0009 a0001c0001t0002g0031 a0001c0001t0002g0051 others(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 | a0001c0001t0057g0256 | 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 | 169 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(166): Show |
244 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(241): 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 | a0001c0001t0009g0006 a0001c0001t0009g0032 a0001c0001t0009g0153 others(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 | 170 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(167): Show |
245 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(242): 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 | a0001c0001t0040g0056 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0113 a0001c0001t0001g0119 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0019 others(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 | a0001c0001t0002g0050 a0001c0001t0002g0274 a0001c0001t0002g0285 others(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 | a0001c0001t0006g0214 a0001c0001t0006g0215 a0001c0001t0006g0296 others(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 | a0001c0001t0019g0053 a0001c0001t0019g0297 a0001c0001t0019g0299 others(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 | a0001c0001t0005g0003 a0001c0001t0005g0033 a0001c0001t0005g0034 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(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 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0030g0135 |
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 | 27 | a0001c0001t0002g0273 a0001c0001t0011g0048 a0001c0001t0011g0049 others(24): Show |
38 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(35): 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 | a0001c0001t0063g0141 | 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 | a0001c0001t0001g0019 a0001c0001t0001g0123 |
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 | a0001c0001t0051g0140 | 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 | 109 | a0001c0001t0002g0273 a0001c0001t0003g0001 a0001c0001t0003g0013 others(106): Show |
152 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(149): 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 | 109 | a0001c0001t0002g0273 a0001c0001t0003g0001 a0001c0001t0003g0013 others(106): Show |
152 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.19-5361A>T | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3835379 | |||||||
| chr12:3835559 | T | C | 110 | a0001c0001t0002g0273 a0001c0001t0003g0001 a0001c0001t0003g0013 others(107): Show |
157 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(154): 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 | a0001c0001t0034g0136 a0001c0001t0034g0137 |
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 | 16 | a0001c0001t0002g0273 a0001c0001t0011g0048 a0001c0001t0011g0049 others(13): Show |
22 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(19): Show |
intron_variant | MODIFIER | c.19-5598T>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3835616 | |||||||
| chr12:3835658 | T | C | 115 | a0001c0001t0002g0273 a0001c0001t0003g0001 a0001c0001t0003g0013 others(112): Show |
163 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(160): 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 | a0001c0001t0009g0006 a0001c0001t0009g0153 a0001c0001t0009g0155 others(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 | a0001c0001t0063g0141 | 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 | a0001c0001t0001g0017 a0001c0001t0001g0126 |
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 | a0001c0001t0051g0140 | 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 | a0001c0001t0051g0140 | 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 | a0001c0001t0007g0020 a0001c0001t0007g0036 a0001c0001t0007g0037 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(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 | a0001c0001t0057g0256 | 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 | a0001c0001t0001g0124 a0001c0001t0001g0125 |
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 | 111 | a0001c0001t0003g0001 a0001c0001t0003g0013 a0001c0001t0003g0014 others(108): Show |
158 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(155): 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 | a0001c0001t0009g0006 a0001c0001t0009g0158 a0001c0001t0073g0154 |
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 | a0001c0001t0055g0263 | 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 | a0001c0001t0014g0183 a0001c0001t0015g0012 a0001c0001t0015g0030 |
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 | 23 | a0001c0001t0011g0048 a0001c0001t0011g0049 a0001c0001t0011g0168 others(20): Show |
33 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(30): 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 | a0001c0001t0008g0295 a0001c0001t0010g0027 a0001c0001t0010g0059 others(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 | a0001c0001t0051g0140 | 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 | 107 | a0001c0001t0002g0043 a0001c0001t0003g0001 a0001c0001t0003g0013 others(104): Show |
154 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(151): 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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(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 | 185 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(182): Show |
270 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(267): 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 | 114 | a0001c0001t0002g0043 a0001c0001t0002g0273 a0001c0001t0003g0001 others(111): Show |
162 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(159): 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 | 21 | a0001c0001t0011g0048 a0001c0001t0011g0049 a0001c0001t0011g0168 others(18): Show |
27 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(24): 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 | a0001c0001t0040g0056 | 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 | a0001c0001t0007g0020 a0001c0001t0007g0036 a0001c0001t0007g0037 others(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 | a0001c0001t0019g0053 a0001c0001t0019g0297 a0001c0001t0019g0299 others(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 | a0001c0001t0003g0014 a0001c0001t0035g0097 |
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 | 112 | a0001c0001t0002g0116 a0001c0001t0003g0001 a0001c0001t0003g0013 others(109): Show |
158 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(155): 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 | a0001c0001t0002g0009 a0001c0001t0002g0031 a0001c0001t0002g0051 others(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 | a0001c0001t0005g0209 a0001c0001t0005g0229 |
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 | a0001c0001t0002g0273 a0001c0001t0008g0052 |
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 | 119 | a0001c0001t0002g0043 a0001c0001t0003g0001 a0001c0001t0003g0013 others(116): Show |
172 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(169): 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 | a0001c0001t0003g0001 a0001c0001t0003g0013 a0001c0001t0003g0014 others(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 | 270 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(267): Show |
377 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(374): 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 | a0001c0001t0007g0020 a0001c0001t0007g0036 a0001c0001t0007g0037 others(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 | a0001c0001t0064g0148 | 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 | a0001c0001t0002g0043 a0001c0001t0015g0012 |
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 | a0001c0001t0033g0044 a0001c0001t0065g0211 a0001c0001t0066g0212 |
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 | 15 | a0001c0001t0002g0273 a0001c0001t0011g0048 a0001c0001t0011g0049 others(12): Show |
21 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(18): 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 | a0001c0001t0019g0053 a0001c0001t0019g0297 a0001c0001t0019g0299 others(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 | a0001c0001t0002g0022 a0001c0001t0004g0232 |
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 | a0001c0001t0033g0044 a0001c0001t0065g0211 a0001c0001t0066g0212 |
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 | a0001c0001t0005g0003 a0001c0001t0005g0033 a0001c0001t0005g0034 others(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 | 187 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(184): Show |
272 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(269): Show |
intron_variant | MODIFIER | c.19-10998C>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3841016 | |||||||
| chr12:3841018 | C | T | 187 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(184): Show |
272 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(269): 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 | a0001c0001t0003g0001 a0001c0001t0003g0013 a0001c0001t0003g0014 others(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 | a0001c0001t0010g0065 a0001c0001t0010g0066 |
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 | a0001c0001t0016g0008 a0001c0001t0016g0269 a0001c0001t0076g0268 |
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 | a0001c0001t0051g0140 | 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 | a0001c0001t0022g0185 a0001c0001t0022g0186 a0001c0001t0022g0188 others(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 | a0001c0001t0077g0284 | 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 | 137 | a0001c0001t0002g0043 a0001c0001t0002g0273 a0001c0001t0003g0001 others(134): Show |
196 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(193): 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 | a0001c0001t0010g0065 a0001c0001t0010g0066 |
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 | 22 | a0001c0001t0002g0273 a0001c0001t0011g0048 a0001c0001t0011g0049 others(19): Show |
28 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(25): 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 | 21 | a0001c0001t0011g0048 a0001c0001t0011g0049 a0001c0001t0011g0168 others(18): Show |
27 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(24): Show |
intron_variant | MODIFIER | c.19-12010G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3842028 | |||||||
| chr12:3842143 | A | G | 110 | a0001c0001t0002g0043 a0001c0001t0003g0001 a0001c0001t0003g0013 others(107): Show |
158 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(155): 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 | a0001c0001t0003g0001 a0001c0001t0003g0013 a0001c0001t0003g0014 others(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 | a0001c0001t0051g0140 | 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 | a0001c0001t0002g0043 a0001c0001t0015g0012 a0001c0001t0015g0030 |
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 | a0001c0001t0005g0003 a0001c0001t0005g0033 a0001c0001t0005g0034 others(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 | a0001c0001t0005g0003 a0001c0001t0005g0033 a0001c0001t0005g0034 others(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 | a0001c0001t0003g0001 a0001c0001t0003g0013 a0001c0001t0003g0014 others(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 | a0001c0001t0003g0001 a0001c0001t0003g0013 a0001c0001t0003g0014 others(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 | a0001c0001t0071g0139 | 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 | a0001c0001t0064g0148 | 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 | a0001c0001t0034g0136 a0001c0001t0034g0137 |
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 | a0001c0001t0070g0147 a0001c0001t0071g0139 |
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 | a0001c0001t0072g0230 | 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 | a0001c0001t0011g0168 a0001c0001t0014g0165 a0001c0001t0014g0166 others(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 | a0001c0001t0011g0168 a0001c0001t0014g0165 a0001c0001t0014g0166 others(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 | a0001c0001t0006g0004 a0001c0001t0006g0021 a0001c0001t0006g0045 others(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 | 132 | a0001c0001t0003g0001 a0001c0001t0003g0013 a0001c0001t0003g0014 others(129): Show |
186 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(183): 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 | a0001c0001t0003g0090 a0001c0001t0003g0091 |
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 | a0001c0001t0071g0139 | 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 | a0001c0001t0014g0165 a0001c0001t0014g0166 a0001c0001t0014g0169 others(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 | 105 | a0001c0001t0002g0273 a0001c0001t0003g0001 a0001c0001t0003g0013 others(102): Show |
147 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(144): 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 | a0001c0001t0003g0001 a0001c0001t0003g0013 a0001c0001t0003g0014 others(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 | 140 | a0001c0001t0002g0043 a0001c0001t0002g0273 a0001c0001t0003g0001 others(137): Show |
200 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(197): Show |
intron_variant | MODIFIER | c.19-15349G>A | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3845367 | |||||||
| chr12:3845390 | T | C | 111 | a0001c0001t0002g0043 a0001c0001t0002g0273 a0001c0001t0003g0001 others(108): Show |
159 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(156): 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 | a0001c0001t0070g0147 | 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 | 140 | a0001c0001t0002g0043 a0001c0001t0002g0273 a0001c0001t0003g0001 others(137): Show |
200 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(197): 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 | a0001c0001t0007g0020 a0001c0001t0007g0036 a0001c0001t0007g0037 others(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 | a0001c0001t0007g0037 a0001c0001t0007g0192 a0001c0001t0007g0195 others(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 | a0001c0001t0019g0053 a0001c0001t0019g0297 a0001c0001t0019g0299 others(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 | 140 | a0001c0001t0002g0043 a0001c0001t0002g0273 a0001c0001t0003g0001 others(137): Show |
200 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(197): 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 | a0001c0001t0019g0053 a0001c0001t0019g0297 a0001c0001t0019g0299 others(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 | a0001c0001t0051g0140 | 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 | a0001c0001t0064g0148 | 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 | a0001c0001t0009g0153 a0001c0001t0009g0155 a0001c0001t0009g0157 others(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 | a0001c0001t0002g0022 a0001c0001t0002g0024 a0001c0001t0002g0239 others(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 | a0001c0001t0003g0001 a0001c0001t0003g0013 a0001c0001t0003g0014 others(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 | a0001c0001t0007g0020 a0001c0001t0007g0036 a0001c0001t0007g0037 others(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 | 22 | a0001c0001t0002g0273 a0001c0001t0011g0048 a0001c0001t0011g0049 others(19): Show |
28 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(25): 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 | a0001c0001t0002g0239 a0001c0001t0004g0238 a0001c0001t0005g0172 others(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 | 140 | a0001c0001t0002g0043 a0001c0001t0002g0273 a0001c0001t0003g0001 others(137): Show |
200 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(197): 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 | a0001c0001t0004g0160 a0001c0001t0009g0006 a0001c0001t0009g0032 others(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 | a0001c0001t0051g0140 | 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 | 104 | a0001c0001t0002g0273 a0001c0001t0003g0001 a0001c0001t0003g0013 others(101): Show |
146 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(143): 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 | a0001c0001t0006g0004 a0001c0001t0006g0021 a0001c0001t0006g0045 others(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 | a0001c0001t0005g0040 a0001c0001t0005g0041 a0001c0001t0005g0042 others(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 | a0001c0001t0006g0004 a0001c0001t0006g0021 a0001c0001t0006g0045 others(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 | a0001c0001t0051g0140 | 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 | 186 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(183): Show |
272 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(269): 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 | a0001c0001t0051g0140 | 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 | a0001c0001t0051g0140 | 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 | a0001c0001t0002g0043 a0001c0001t0010g0075 a0001c0001t0011g0168 others(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 | a0001c0001t0005g0181 a0001c0001t0005g0182 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(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 | a0001c0001t0007g0020 a0001c0001t0007g0036 a0001c0001t0007g0037 others(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 | a0001c0001t0002g0031 a0001c0001t0003g0001 a0001c0001t0003g0013 others(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 | a0001c0001t0053g0291 | 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 | a0001c0001t0002g0043 a0001c0001t0011g0168 a0001c0001t0014g0165 others(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 | 15 | a0001c0001t0011g0048 a0001c0001t0011g0049 a0001c0001t0011g0265 others(12): Show |
21 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(18): 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 | 230 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(227): Show |
326 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(323): 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 | a0001c0001t0002g0031 a0001c0001t0002g0043 a0001c0001t0003g0001 others(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 | a0001c0001t0004g0254 a0001c0001t0048g0253 |
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 | a0001c0001t0019g0053 a0001c0001t0019g0297 a0001c0001t0019g0299 others(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 | a0001c0001t0034g0136 a0001c0001t0034g0137 |
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 | a0001c0001t0007g0020 a0001c0001t0007g0036 a0001c0001t0007g0037 others(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 | 185 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(182): Show |
271 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(268): 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 | a0001c0001t0010g0027 a0001c0001t0010g0064 |
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 | a0001c0001t0072g0230 | 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 | a0001c0001t0002g0116 a0001c0001t0008g0016 a0001c0001t0008g0018 others(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 | a0001c0001t0064g0148 | 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 | a0001c0001t0019g0053 a0001c0001t0019g0297 a0001c0001t0019g0299 others(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 | a0001c0001t0004g0251 a0001c0001t0021g0083 a0001c0001t0062g0235 |
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 | a0001c0001t0019g0053 a0001c0001t0019g0297 a0001c0001t0019g0299 others(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 | a0001c0001t0003g0100 a0001c0001t0008g0295 a0001c0001t0010g0027 others(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 | a0001c0001t0011g0270 a0001c0001t0011g0271 a0001c0001t0011g0272 others(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 | a0001c0001t0003g0001 a0001c0001t0003g0013 a0001c0001t0003g0014 others(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 | a0001c0001t0070g0147 a0001c0001t0071g0139 |
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 | a0001c0001t0022g0185 a0001c0001t0022g0186 a0001c0001t0022g0188 others(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 | a0001c0001t0005g0003 a0001c0001t0005g0033 a0001c0001t0005g0034 others(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 | a0001c0001t0064g0148 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(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 | a0001c0001t0033g0044 a0001c0001t0065g0211 a0001c0001t0066g0212 |
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 | a0001c0001t0002g0281 a0001c0001t0002g0283 a0001c0001t0004g0282 |
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 | a0001c0001t0011g0168 a0001c0001t0014g0165 a0001c0001t0014g0166 others(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 | a0001c0001t0051g0140 | 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 | a0001c0001t0002g0043 a0001c0001t0003g0001 a0001c0001t0003g0013 others(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 | a0001c0001t0006g0004 a0001c0001t0006g0021 a0001c0001t0006g0045 others(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 | a0001c0001t0003g0001 a0001c0001t0003g0013 a0001c0001t0003g0014 others(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 | a0001c0001t0034g0136 a0001c0001t0034g0137 a0001c0001t0070g0147 others(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 | a0001c0001t0072g0230 | 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 | a0001c0001t0064g0148 | 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 | a0001c0001t0002g0043 a0001c0001t0003g0001 a0001c0001t0003g0013 others(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 | a0001c0001t0014g0165 a0001c0001t0014g0166 a0001c0001t0014g0169 others(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 | a0001c0001t0002g0043 a0001c0001t0003g0001 a0001c0001t0003g0013 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(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 | a0001c0001t0006g0004 a0001c0001t0006g0021 a0001c0001t0006g0045 others(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 | a0001c0001t0004g0254 a0001c0001t0048g0253 |
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 | a0001c0001t0002g0031 a0001c0001t0003g0145 |
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 | a0001c0001t0005g0041 a0001c0001t0005g0210 |
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 | a0001c0001t0019g0053 a0001c0001t0019g0297 a0001c0001t0019g0299 others(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 | a0001c0001t0011g0168 a0001c0001t0014g0165 a0001c0001t0014g0166 others(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 | a0001c0001t0002g0278 a0001c0001t0007g0020 a0001c0001t0007g0036 others(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 | a0001c0001t0007g0020 a0001c0001t0007g0036 a0001c0001t0007g0037 others(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 | a0001c0001t0007g0020 a0001c0001t0007g0036 a0001c0001t0007g0037 others(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 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0030g0135 |
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 | 109 | a0001c0001t0002g0031 a0001c0001t0002g0043 a0001c0001t0002g0273 others(106): Show |
157 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(154): 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 | a0001c0001t0034g0136 a0001c0001t0034g0137 |
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 | a0001c0001t0064g0148 | 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 | a0001c0001t0006g0004 a0001c0001t0006g0021 a0001c0001t0006g0045 others(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 | 141 | a0001c0001t0002g0031 a0001c0001t0002g0043 a0001c0001t0003g0001 others(138): Show |
202 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(199): 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 | 108 | a0001c0001t0002g0031 a0001c0001t0002g0043 a0001c0001t0003g0001 others(105): Show |
156 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(153): 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 | a0001c0001t0003g0100 a0001c0001t0004g0255 |
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 | a0001c0001t0005g0040 a0001c0001t0005g0041 a0001c0001t0005g0042 others(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 | a0001c0001t0033g0044 a0001c0001t0065g0211 a0001c0001t0066g0212 |
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 | a0001c0001t0002g0277 a0001c0001t0008g0295 a0001c0001t0064g0148 |
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 | a0001c0001t0057g0256 | 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 | a0001c0001t0002g0031 a0001c0001t0003g0001 a0001c0001t0003g0013 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(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 | a0001c0001t0002g0050 a0001c0001t0002g0274 a0001c0001t0002g0292 others(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 | a0001c0001t0002g0031 a0001c0001t0003g0001 a0001c0001t0003g0013 others(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 | a0001c0001t0002g0116 a0001c0001t0008g0016 a0001c0001t0008g0018 others(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 | a0001c0001t0002g0031 a0001c0001t0003g0001 a0001c0001t0003g0013 others(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 | a0001c0001t0002g0031 a0001c0001t0003g0001 a0001c0001t0003g0013 others(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 | a0001c0001t0002g0031 a0001c0001t0003g0001 a0001c0001t0003g0013 others(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 | a0001c0001t0006g0214 a0001c0001t0006g0215 a0001c0001t0006g0296 others(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 | 207 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(204): Show |
301 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(298): 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 | a0001c0001t0002g0022 a0001c0001t0002g0024 a0001c0001t0002g0239 others(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 | a0001c0001t0002g0031 a0001c0001t0002g0138 a0001c0001t0003g0001 others(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 | a0001c0001t0002g0043 a0001c0001t0015g0012 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(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 | a0001c0001t0002g0031 a0001c0001t0002g0043 a0001c0001t0003g0001 others(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 | a0001c0001t0071g0139 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0019 others(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 | a0001c0001t0002g0031 a0001c0001t0003g0001 a0001c0001t0003g0013 others(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 | a0001c0001t0038g0054 | 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 | a0001c0001t0033g0044 a0001c0001t0065g0211 a0001c0001t0066g0212 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(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 | a0001c0001t0006g0004 a0001c0001t0006g0021 a0001c0001t0006g0045 others(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 | a0001c0001t0034g0136 a0001c0001t0034g0137 |
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 | a0001c0001t0002g0031 a0001c0001t0003g0001 a0001c0001t0003g0013 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(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 | a0001c0001t0006g0214 a0001c0001t0006g0215 a0001c0001t0006g0296 others(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 | a0001c0001t0003g0001 a0001c0001t0003g0013 a0001c0001t0003g0014 others(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 | a0001c0001t0007g0020 a0001c0001t0007g0036 a0001c0001t0007g0037 others(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 | a0001c0001t0002g0051 a0001c0001t0002g0275 a0001c0001t0002g0276 |
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 | a0001c0001t0019g0053 a0001c0001t0019g0297 a0001c0001t0019g0299 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(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 | a0001c0001t0005g0003 a0001c0001t0005g0033 a0001c0001t0005g0034 others(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 | a0001c0001t0002g0051 a0001c0001t0002g0275 a0001c0001t0002g0276 |
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 | a0001c0001t0002g0031 a0001c0001t0003g0001 a0001c0001t0003g0013 others(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 | 55 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(52): Show |
85 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(82): 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 | a0001c0001t0062g0235 | 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 | a0001c0001t0002g0031 a0001c0001t0003g0001 a0001c0001t0003g0013 others(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 | a0001c0001t0011g0168 a0001c0001t0014g0165 a0001c0001t0014g0166 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(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 | a0001c0001t0002g0031 a0001c0001t0003g0001 a0001c0001t0003g0013 others(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 | a0001c0001t0017g0010 a0001c0001t0023g0161 a0001c0001t0023g0162 others(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 | a0001c0001t0002g0050 a0001c0001t0002g0274 |
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 | a0001c0001t0002g0031 a0001c0001t0003g0001 a0001c0001t0003g0013 others(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 | a0001c0001t0002g0031 a0001c0001t0003g0001 a0001c0001t0003g0013 others(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 | a0001c0001t0002g0043 a0001c0001t0015g0012 a0001c0001t0015g0030 others(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 | a0001c0001t0006g0004 a0001c0001t0006g0021 a0001c0001t0006g0045 others(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 | a0001c0001t0019g0053 a0001c0001t0019g0297 a0001c0001t0019g0299 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(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 | a0001c0001t0003g0001 a0001c0001t0003g0013 a0001c0001t0003g0014 others(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 | 110 | a0001c0001t0002g0043 a0001c0001t0003g0001 a0001c0001t0003g0013 others(107): Show |
158 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(155): 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 | a0001c0001t0070g0147 | 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 | a0001c0001t0005g0181 a0001c0001t0005g0182 |
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 | a0001c0001t0028g0035 a0001c0001t0072g0230 |
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 | a0001c0001t0005g0209 a0001c0001t0005g0229 a0001c0001t0043g0058 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(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 | a0001c0001t0019g0053 a0001c0001t0019g0297 a0001c0001t0019g0299 others(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 | a0001c0001t0002g0031 a0001c0001t0003g0001 a0001c0001t0003g0013 others(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 | 166 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(163): Show |
246 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(243): Show |
intron_variant | MODIFIER | c.18+7322dupA | PARP11 | ENSG00000111224.14 | transcript | ENST00000228820.9 | protein_coding | 1/7 | chr12 | 3865889 | |||||||
| chr12:3865995 | C | T | 1 | a0001c0001t0044g0085 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(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 | a0001c0001t0019g0053 a0001c0001t0019g0297 a0001c0001t0019g0299 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(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 | a0001c0001t0003g0001 a0001c0001t0003g0013 a0001c0001t0003g0014 others(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 | a0001c0001t0007g0020 a0001c0001t0007g0036 a0001c0001t0007g0037 others(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 | 128 | a0001c0001t0002g0273 a0001c0001t0003g0001 a0001c0001t0003g0013 others(125): Show |
179 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(176): 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 | a0001c0001t0005g0040 a0001c0001t0005g0041 a0001c0001t0005g0042 others(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 | a0001c0001t0070g0147 a0001c0001t0071g0139 a0001c0001t0072g0230 |
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 | 17 | a0001c0001t0002g0273 a0001c0001t0011g0048 a0001c0001t0011g0049 others(14): Show |
23 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(20): 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 | a0001c0001t0072g0230 | 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 | a0001c0001t0070g0147 | 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 | a0001c0001t0005g0040 a0001c0001t0005g0041 a0001c0001t0005g0042 others(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 | a0001c0001t0003g0001 a0001c0001t0003g0013 a0001c0001t0003g0014 others(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 | a0001c0001t0002g0043 a0001c0001t0015g0012 |
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 | a0001c0001t0051g0140 | 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 | a0001c0001t0003g0100 a0001c0001t0008g0295 a0001c0001t0010g0027 others(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 | a0001c0001t0002g0022 a0001c0001t0004g0232 |
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 | a0001c0001t0033g0044 a0001c0001t0065g0211 a0001c0001t0066g0212 |
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 | a0001c0001t0019g0053 a0001c0001t0019g0297 a0001c0001t0019g0299 others(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 | a0001c0001t0002g0022 a0001c0001t0002g0024 a0001c0001t0002g0239 others(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 | a0001c0001t0006g0004 a0001c0001t0006g0021 a0001c0001t0006g0045 others(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 | a0001c0001t0005g0143 a0001c0001t0005g0144 |
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 | a0001c0001t0003g0015 a0001c0001t0003g0105 a0001c0001t0003g0106 others(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 | a0001c0001t0041g0077 | 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 | a0001c0001t0019g0053 a0001c0001t0019g0297 a0001c0001t0019g0299 others(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 | a0001c0001t0072g0230 | 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 | a0001c0001t0002g0022 a0001c0001t0002g0024 a0001c0001t0002g0138 others(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 | a0001c0001t0063g0141 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(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 | a0001c0001t0051g0140 | 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 | a0001c0001t0051g0140 | 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 | a0001c0001t0071g0139 | 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 | a0001c0001t0003g0013 a0001c0001t0003g0029 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(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 | a0001c0001t0008g0108 a0001c0001t0008g0109 a0001c0001t0008g0110 |
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 | a0001c0001t0019g0053 a0001c0001t0019g0297 a0001c0001t0019g0299 others(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 | a0001c0001t0003g0001 a0001c0001t0003g0013 a0001c0001t0003g0014 others(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 |