| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:108719347-108719729 | Common:6; Rare:249; Clinvar (benign):3 | ||||
| chr2:108786587-108786834 | Common:6; Rare:122 | ||||
| chr2:109613609-109613783 | Common:3; Rare:66 | ||||
| chr2:109613846-109614431 | Common:12; Rare:425 | ||||
| chr2:110204958-110205091 | Rare:58; Clinvar:1 | ||||
| chr2:110677997-110678265 | Rare:167 | ||||
| chr2:111120576-111120991 | Common:8; Rare:323 | ||||
| chr2:111122447-111122663 | Common:1; Rare:92 | ||||
| chr2:111884036-111884290 | Common:3; Rare:122 | ||||
| chr2:111898280-111898690 | Common:4; Rare:182 | ||||
| chr2:111898710-111899028 | Common:4; Rare:129; Clinvar:1; Clinvar (benign):4 | ||||
| chr2:112255007-112255187 | Common:3; Rare:151 | ||||
| chr2:112275384-112275654 | Common:2; Rare:180 | ||||
| chr2:112276044-112276316 | Rare:134 | ||||
| chr2:112432634-112433130 | Common:7; Rare:228 |