| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:98346417-98346529 | Rare:37 | ||||
| chr2:98608381-98608665 | Common:1; Rare:120; Clinvar (benign):1 | ||||
| chr2:99141141-99141246 | Common:1; Rare:38 | ||||
| chr2:99141394-99141735 | Common:2; Rare:128 | ||||
| chr2:99154844-99155054 | Common:2; Rare:88; Clinvar (benign):2 | ||||
| chr2:99180979-99181227 | Common:2; Rare:72 | ||||
| chr2:99337203-99337464 | Rare:90 | ||||
| chr2:100417340-100417731 | Rare:116 | ||||
| chr2:100562639-100563067 | Common:5; Rare:128 | ||||
| chr2:101002156-101002318 | Rare:63 | ||||
| chr2:101002496-101002798 | Rare:71 | ||||
| chr2:102104467-102104623 | Rare:30 | ||||
| chr2:102736844-102736955 | Common:1; Rare:49 | ||||
| chr2:105037867-105038106 | Common:3; Rare:84 | ||||
| chr2:105337211-105337632 | Common:5; Rare:143 |