| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:97645780-97646126 | Common:3; Rare:108 | ||||
| chr2:98608434-98608649 | Common:1; Rare:96 | ||||
| chr2:99154877-99155050 | Common:1; Rare:72; Clinvar (benign):2 | ||||
| chr2:99180960-99181239 | Common:2; Rare:83 | ||||
| chr2:99337203-99337466 | Rare:91 | ||||
| chr2:100417352-100417705 | Rare:103 | ||||
| chr2:100562855-100563050 | Common:3; Rare:64 | ||||
| chr2:101002142-101002629 | Rare:152 | ||||
| chr2:102736846-102736949 | Common:1; Rare:44 | ||||
| chr2:105037814-105038117 | Common:4; Rare:107 | ||||
| chr2:105337457-105337590 | Common:1; Rare:66 | ||||
| chr2:105398961-105399152 | Rare:68 | ||||
| chr2:105438494-105438604 | Rare:26 | ||||
| chr2:106194243-106194593 | Common:6; Rare:145 | ||||
| chr2:108449097-108449260 | Rare:58 |