| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:97589778-97590008 | Common:5; Rare:57 | ||||
| chr2:97645806-97646095 | Common:2; Rare:88 | ||||
| chr2:98608442-98608636 | Common:1; Rare:86 | ||||
| chr2:99141128-99141492 | Common:1; Rare:135 | ||||
| chr2:99141528-99141735 | Common:2; Rare:77 | ||||
| chr2:99154883-99155037 | Common:1; Rare:64; Clinvar (benign):1 | ||||
| chr2:99180956-99181239 | Common:2; Rare:85 | ||||
| chr2:99337253-99337454 | Rare:69 | ||||
| chr2:100562901-100563061 | Rare:54 | ||||
| chr2:101002124-101002508 | Rare:132 | ||||
| chr2:102736855-102736955 | Common:1; Rare:37 | ||||
| chr2:105037870-105038110 | Common:3; Rare:87 | ||||
| chr2:105337454-105337602 | Common:1; Rare:74 | ||||
| chr2:105398987-105399192 | Rare:71 | ||||
| chr2:106194243-106194593 | Common:6; Rare:145 |