| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:101697435-101698143 | Common:5; Rare:229 | ||||
| chr12:101698154-101698319 | Common:1; Rare:40 | ||||
| chr12:101698385-101698596 | Common:2; Rare:37 | ||||
| chr12:101830732-101830994 | Common:2; Rare:106; Clinvar (benign):2 | ||||
| chr12:101877093-101877805 | Common:10; Rare:162 | ||||
| chr12:101877997-101878087 | Rare:15 | ||||
| chr12:102061603-102061681 | Common:2; Rare:17 | ||||
| chr12:102061748-102061836 | Rare:24 | ||||
| chr12:102061878-102062233 | Common:1; Rare:101 | ||||
| chr12:102120005-102120561 | Common:4; Rare:173 | ||||
| chr12:103840813-103840845 | Rare:7 | ||||
| chr12:103840881-103841561 | Common:8; Rare:201 | ||||
| chr12:103930761-103930858 | Common:2; Rare:21 | ||||
| chr12:103956629-103956822 | Rare:60 | ||||
| chr12:103956902-103957006 | Rare:13 |