| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:98444760-98445074 | Common:1; Rare:119 | ||||
| chr2:98608305-98608659 | Common:1; Rare:148; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:98731062-98731330 | Common:3; Rare:93 | ||||
| chr2:99141141-99141345 | Common:1; Rare:78 | ||||
| chr2:99141415-99141735 | Common:2; Rare:122 | ||||
| chr2:99154845-99155050 | Common:2; Rare:88; Clinvar (benign):2 | ||||
| chr2:99180971-99181248 | Common:2; Rare:81 | ||||
| chr2:99337260-99337585 | Rare:116 | ||||
| chr2:100309193-100309495 | Common:3; Rare:57 | ||||
| chr2:100322204-100322253 | Rare:14 | ||||
| chr2:100322444-100322531 | Common:2; Rare:18 | ||||
| chr2:100322540-100322581 | Rare:13 | ||||
| chr2:100562732-100563050 | Common:3; Rare:101 | ||||
| chr2:101002162-101002318 | Rare:61 | ||||
| chr2:101252658-101253198 | Common:7; Rare:180 |