| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:12356709-12357622 | Common:7; Rare:316 | ||||
| chr12:12357629-12357827 | Rare:51 | ||||
| chr12:12561147-12561356 | Common:1; Rare:41 | ||||
| chr12:12561374-12561600 | Common:2; Rare:50 | ||||
| chr12:12561610-12562339 | Common:1; Rare:189 | ||||
| chr12:12562341-12562362 | Rare:8 | ||||
| chr12:12562366-12562723 | Common:3; Rare:82 | ||||
| chr12:12562756-12562903 | Rare:45 | ||||
| chr12:12611546-12611974 | Common:3; Rare:123 | ||||
| chr12:12611995-12612293 | Common:2; Rare:88 | ||||
| chr12:12612326-12612343 | Rare:4 | ||||
| chr12:12696101-12696410 | Common:2; Rare:72 | ||||
| chr12:12696609-12696828 | Rare:58 | ||||
| chr12:12716640-12716715 | Rare:15 | ||||
| chr12:12716920-12717541 | Common:3; Rare:194; Clinvar:2; Clinvar (benign):1 |