| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:111766794-111766980 | Rare:57 | ||||
| chr12:111841855-111842233 | Common:3; Rare:104 | ||||
| chr12:112013123-112013467 | Common:1; Rare:122 | ||||
| chr12:112108735-112108813 | Rare:23 | ||||
| chr12:113185429-113185769 | Common:9; Rare:127 | ||||
| chr12:113966318-113966491 | Common:5; Rare:58 | ||||
| chr12:114684162-114684350 | Rare:47 | ||||
| chr12:118135959-118136195 | Common:2; Rare:70 | ||||
| chr12:118372862-118373193 | Common:1; Rare:86 | ||||
| chr12:120116725-120116928 | Common:2; Rare:65 | ||||
| chr12:120201081-120201360 | Common:2; Rare:89 | ||||
| chr12:120438018-120438229 | Rare:93; Clinvar (benign):2 | ||||
| chr12:120446301-120446474 | Common:1; Rare:70 | ||||
| chr12:120469445-120469895 | Common:6; Rare:146 | ||||
| chr12:120495843-120496222 | Common:8; Rare:127 |