| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:120253040-120253580 | Common:2; Rare:134 | ||||
| chr2:120735568-120735893 | Common:13; Rare:105 | ||||
| chr2:121530599-121530946 | Common:7; Rare:195; Clinvar (pathogenic):12 | ||||
| chr2:121649421-121649832 | Common:2; Rare:117 | ||||
| chr2:121650058-121650163 | Rare:27 | ||||
| chr2:121736855-121737281 | Common:5; Rare:158 | ||||
| chr2:121755402-121755704 | Common:3; Rare:93 | ||||
| chr2:124025171-124025288 | Common:2; Rare:39 | ||||
| chr2:126655806-126656073 | Common:1; Rare:64 | ||||
| chr2:127107036-127107365 | Common:4; Rare:102; Clinvar:7; Clinvar (benign):1 | ||||
| chr2:127219662-127220024 | Common:2; Rare:65 | ||||
| chr2:127220252-127220457 | Rare:42 | ||||
| chr2:127294073-127294313 | Common:2; Rare:88; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:127387231-127387535 | Common:4; Rare:101 | ||||
| chr2:127387918-127388244 | Common:9; Rare:144 |