| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:105236036-105236314 | Common:2; Rare:122 | ||||
| chr12:107685675-107685860 | Common:1; Rare:64 | ||||
| chr12:108562396-108562673 | Common:8; Rare:118; Clinvar:2; Clinvar (benign):4 | ||||
| chr12:109052488-109052645 | Common:3; Rare:46 | ||||
| chr12:109097851-109098226 | Common:5; Rare:118 | ||||
| chr12:109477293-109477643 | Common:3; Rare:82 | ||||
| chr12:109573472-109573814 | Common:3; Rare:102; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr12:109996220-109996456 | Common:2; Rare:68 | ||||
| chr12:110281024-110281193 | Rare:66 | ||||
| chr12:110502058-110502200 | Common:1; Rare:54 | ||||
| chr12:111685857-111686127 | Rare:99 | ||||
| chr12:111841885-111841998 | Common:2; Rare:37 | ||||
| chr12:112013110-112013460 | Common:1; Rare:124 | ||||
| chr12:112125377-112125574 | Rare:52 | ||||
| chr12:113185440-113185729 | Common:7; Rare:108 |