| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:112561872-112562065 | Common:1; Rare:58 | ||||
| chr3:112990662-112991005 | Common:3; Rare:86 | ||||
| chr3:112991234-112991469 | Common:3; Rare:102 | ||||
| chr3:113019382-113019536 | Common:3; Rare:45 | ||||
| chr3:113019645-113019868 | Common:3; Rare:69 | ||||
| chr3:113515114-113515257 | Rare:42 | ||||
| chr3:113532259-113532600 | Common:4; Rare:60 | ||||
| chr3:113746142-113746454 | Rare:119 | ||||
| chr3:113746976-113747088 | Common:3; Rare:15 | ||||
| chr3:114056486-114056814 | Common:2; Rare:128 | ||||
| chr3:114307623-114307708 | Common:1; Rare:14 | ||||
| chr3:114454878-114454926 | Rare:5 | ||||
| chr3:119294500-119294690 | Rare:37; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:119468848-119468995 | Rare:54 | ||||
| chr3:119498403-119498620 | Common:3; Rare:75 |