| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:97094820-97094966 | Common:1; Rare:30 | ||||
| chr2:97113493-97113642 | Rare:34 | ||||
| chr2:97589703-97589974 | Common:7; Rare:73 | ||||
| chr2:97590281-97590528 | Common:1; Rare:51 | ||||
| chr2:97645876-97646114 | Common:3; Rare:76 | ||||
| chr2:97713428-97713640 | Common:1; Rare:28; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:98444734-98445021 | Common:1; Rare:113 | ||||
| chr2:98608420-98608636 | Common:1; Rare:93; Clinvar (benign):1 | ||||
| chr2:99141529-99141707 | Common:2; Rare:72 | ||||
| chr2:99154871-99155121 | Common:4; Rare:100; Clinvar (benign):3 | ||||
| chr2:99180989-99181227 | Common:2; Rare:70 | ||||
| chr2:99337226-99337433 | Rare:69 | ||||
| chr2:100142477-100142713 | Common:4; Rare:42 | ||||
| chr2:100562855-100563046 | Common:3; Rare:63 | ||||
| chr2:101002162-101002325 | Rare:63 |