| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27032862-27033017 | Rare:60 | ||||
| chr2:27051614-27051681 | Rare:19 | ||||
| chr2:27086601-27086792 | Common:1; Rare:54; Clinvar (benign):1 | ||||
| chr2:27211775-27212106 | Common:3; Rare:116 | ||||
| chr2:27212246-27212437 | Common:2; Rare:100 | ||||
| chr2:27217318-27217501 | Rare:79 | ||||
| chr2:27323039-27323126 | Rare:21; Clinvar (benign):1 | ||||
| chr2:27356743-27357200 | Common:2; Rare:139 | ||||
| chr2:27370247-27370648 | Common:1; Rare:162 | ||||
| chr2:27380762-27381017 | Common:1; Rare:83 | ||||
| chr2:27442215-27442439 | Common:1; Rare:86 | ||||
| chr2:27583003-27583120 | Rare:44 | ||||
| chr2:27628958-27629108 | Common:1; Rare:84 | ||||
| chr2:27663342-27663911 | Rare:176 | ||||
| chr2:27664247-27664416 | Common:1; Rare:48 |