| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:99337253-99337469 | Rare:78 | ||||
| chr2:100105369-100105479 | Rare:31 | ||||
| chr2:100562855-100563070 | Common:3; Rare:74 | ||||
| chr2:101252646-101252907 | Common:5; Rare:88 | ||||
| chr2:102736821-102736974 | Common:1; Rare:74 | ||||
| chr2:105037833-105038106 | Common:3; Rare:94 | ||||
| chr2:105337443-105337606 | Common:2; Rare:81 | ||||
| chr2:106194190-106194568 | Common:6; Rare:162 | ||||
| chr2:106887250-106887456 | Rare:41 | ||||
| chr2:108288701-108289067 | Common:2; Rare:62 | ||||
| chr2:108449104-108449277 | Rare:69 | ||||
| chr2:108534140-108534534 | Common:8; Rare:158 | ||||
| chr2:108719388-108719654 | Common:3; Rare:113; Clinvar (benign):2 | ||||
| chr2:109613865-109614008 | Common:2; Rare:50 | ||||
| chr2:111122449-111122774 | Common:3; Rare:132 |