| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:11648950-11649450 | Common:2; Rare:144 | ||||
| chr12:11649588-11649789 | Rare:52 | ||||
| chr12:11649907-11650124 | Rare:61 | ||||
| chr12:12266959-12267438 | Common:9; Rare:194 | ||||
| chr12:12356945-12357200 | Common:4; Rare:124 | ||||
| chr12:12561143-12561277 | Common:1; Rare:28 | ||||
| chr12:12562789-12562904 | Rare:35 | ||||
| chr12:12611567-12612040 | Common:3; Rare:140 | ||||
| chr12:12696123-12696498 | Common:2; Rare:86 | ||||
| chr12:12716966-12717621 | Common:3; Rare:211; Clinvar:3; Clinvar (benign):3 | ||||
| chr12:12718032-12718239 | Common:1; Rare:106; Clinvar:24; Clinvar (benign):19; Clinvar (pathogenic):2 | ||||
| chr12:12725083-12725552 | Common:3; Rare:115 | ||||
| chr12:12725558-12725875 | Common:4; Rare:70 | ||||
| chr12:12784836-12785236 | Common:5; Rare:125 | ||||
| chr12:12813182-12813419 | Common:2; Rare:73 |