| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:111685776-111686114 | Rare:128 | ||||
| chr12:111766762-111766977 | Rare:62 | ||||
| chr12:111841877-111842233 | Common:3; Rare:96 | ||||
| chr12:112013129-112013467 | Common:1; Rare:119 | ||||
| chr12:112906810-112906995 | Common:1; Rare:30 | ||||
| chr12:113185447-113185739 | Common:7; Rare:107 | ||||
| chr12:113966286-113966540 | Common:9; Rare:87 | ||||
| chr12:114407947-114408198 | Common:1; Rare:45; Clinvar (benign):2 | ||||
| chr12:114684146-114684350 | Rare:53 | ||||
| chr12:118135941-118136175 | Common:2; Rare:75 | ||||
| chr12:118372904-118373139 | Common:1; Rare:51 | ||||
| chr12:120194683-120194786 | Rare:37 | ||||
| chr12:120201081-120201354 | Common:2; Rare:88 | ||||
| chr12:120446353-120446474 | Common:1; Rare:55 | ||||
| chr12:120469637-120469880 | Common:3; Rare:88 |