| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:97995510-97996004 | Common:10; Rare:297 | ||||
| chr2:97996052-97996452 | Common:10; Rare:481 | ||||
| chr2:98444619-98445019 | Common:2; Rare:289 | ||||
| chr2:98608190-98608833 | Common:10; Rare:761; Clinvar:1; Clinvar (benign):4 | ||||
| chr2:98608948-98609348 | Common:2; Rare:97 | ||||
| chr2:98730870-98731400 | Common:12; Rare:305 | ||||
| chr2:99141010-99141537 | Common:5; Rare:637 | ||||
| chr2:99141506-99141948 | Common:6; Rare:350 | ||||
| chr2:99154510-99154800 | Rare:95 | ||||
| chr2:99154810-99155188 | Common:21; Rare:696; Clinvar (benign):19 | ||||
| chr2:99155170-99155430 | Common:1; Rare:80 | ||||
| chr2:99180882-99181608 | Common:12; Rare:691 | ||||
| chr2:99335415-99336188 | Common:5; Rare:238 | ||||
| chr2:99336152-99336851 | Common:12; Rare:631 | ||||
| chr2:99336905-99338275 | Common:17; Rare:809 |