| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:100709235-100709695 | Common:6; Rare:140; Clinvar (benign):1 | ||||
| chr3:101513135-101513339 | Common:8; Rare:41 | ||||
| chr3:101574049-101574225 | Rare:57 | ||||
| chr3:101685855-101686157 | Common:4; Rare:79 | ||||
| chr3:101686672-101686884 | Common:2; Rare:88 | ||||
| chr3:101724529-101724654 | Rare:47 | ||||
| chr3:105868882-105869184 | Common:6; Rare:109 | ||||
| chr3:107522873-107523060 | Common:1; Rare:45 | ||||
| chr3:108589395-108589730 | Common:3; Rare:99 | ||||
| chr3:111859480-111859859 | Rare:119 | ||||
| chr3:112561588-112561702 | Rare:39 | ||||
| chr3:112561909-112562085 | Rare:54 | ||||
| chr3:112990909-112991012 | Common:1; Rare:39 | ||||
| chr3:113019400-113019528 | Common:3; Rare:38 | ||||
| chr3:113746065-113746327 | Common:1; Rare:94 |