| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:97094784-97094962 | Common:1; Rare:37 | ||||
| chr2:97645811-97646186 | Common:3; Rare:112 | ||||
| chr2:98608402-98608655 | Common:1; Rare:111; Clinvar (benign):1 | ||||
| chr2:99141146-99141452 | Common:1; Rare:106 | ||||
| chr2:99141512-99141770 | Common:2; Rare:90 | ||||
| chr2:99154873-99155079 | Common:2; Rare:81; Clinvar (benign):3 | ||||
| chr2:99180960-99181233 | Common:2; Rare:82 | ||||
| chr2:99181299-99181433 | Rare:30 | ||||
| chr2:99337304-99337529 | Rare:82 | ||||
| chr2:100562665-100563069 | Common:4; Rare:125 | ||||
| chr2:101002156-101002325 | Rare:65 | ||||
| chr2:102736821-102736939 | Common:1; Rare:59 | ||||
| chr2:105037884-105038184 | Common:4; Rare:108 | ||||
| chr2:105337443-105337606 | Common:2; Rare:81 | ||||
| chr2:105398978-105399194 | Rare:78 |