| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:112013121-112013468 | Common:1; Rare:124 | ||||
| chr12:112409542-112409707 | Common:1; Rare:55 | ||||
| chr12:112791828-112791948 | Common:4; Rare:35 | ||||
| chr12:113185422-113185748 | Common:8; Rare:129 | ||||
| chr12:113966318-113966527 | Common:8; Rare:73 | ||||
| chr12:117190419-117190605 | Rare:86 | ||||
| chr12:118016588-118016798 | Rare:42 | ||||
| chr12:118135938-118136211 | Common:2; Rare:86 | ||||
| chr12:118190428-118190572 | Rare:28 | ||||
| chr12:118372884-118373165 | Common:1; Rare:65 | ||||
| chr12:118981304-118981541 | Rare:73 | ||||
| chr12:120116828-120116943 | Common:2; Rare:37 | ||||
| chr12:120201085-120201354 | Common:2; Rare:86 | ||||
| chr12:120437850-120438222 | Common:2; Rare:138; Clinvar (benign):2 | ||||
| chr12:120446353-120446474 | Common:1; Rare:55 |