| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:113358777-113358843 | Rare:16 | ||||
| chr12:113358958-113358993 | Rare:3 | ||||
| chr12:113422300-113422483 | Common:2; Rare:44 | ||||
| chr12:113966000-113966167 | Common:1; Rare:41 | ||||
| chr12:113966216-113966550 | Common:10; Rare:108 | ||||
| chr12:114682825-114682955 | Rare:32; Clinvar:3 | ||||
| chr12:114683019-114683215 | Common:1; Rare:60; Clinvar (benign):2 | ||||
| chr12:114683479-114683518 | Rare:5 | ||||
| chr12:114683886-114684411 | Common:5; Rare:129; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:114684493-114684963 | Common:3; Rare:128 | ||||
| chr12:116276438-116276509 | Rare:26 | ||||
| chr12:116276552-116277247 | Common:4; Rare:213; Clinvar (benign):2 | ||||
| chr12:116277345-116277482 | Rare:34 | ||||
| chr12:116277498-116277944 | Common:1; Rare:152 | ||||
| chr12:116559441-116559724 | Common:2; Rare:44 |