| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:121797262-121797419 | Rare:68 | ||||
| chr12:121797542-121797674 | Rare:51 | ||||
| chr12:122855872-122856123 | Common:2; Rare:105 | ||||
| chr12:122856139-122856524 | Common:1; Rare:157 | ||||
| chr12:122856911-122857068 | Common:2; Rare:40 | ||||
| chr12:122860954-122861183 | Common:2; Rare:99 | ||||
| chr12:123630470-123630610 | Rare:32 | ||||
| chr12:127060359-127060617 | Common:4; Rare:85 | ||||
| chr12:127146081-127146394 | Rare:115 | ||||
| chr12:130633857-130634110 | Common:2; Rare:65 | ||||
| chr12:132672284-132672431 | Rare:63; Clinvar:2; Clinvar (benign):8 | ||||
| chr13:19957272-19957451 | Rare:36 | ||||
| chr13:20560741-20560891 | Common:2; Rare:28 | ||||
| chr13:27451241-27451423 | Rare:40 | ||||
| chr13:27968531-27968986 | Common:6; Rare:155 |