| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:144517426-144517796 | Common:6; Rare:93 | ||||
| chr2:144518134-144518203 | Common:1; Rare:14 | ||||
| chr2:144518374-144518499 | Rare:27 | ||||
| chr2:144519348-144519572 | Common:1; Rare:39 | ||||
| chr2:144520136-144520547 | Common:4; Rare:72; Clinvar (benign):1 | ||||
| chr2:148020673-148021125 | Common:2; Rare:107; Clinvar (benign):2 | ||||
| chr2:148021495-148021671 | Rare:38 | ||||
| chr2:149038644-149038787 | Common:1; Rare:52 | ||||
| chr2:149587275-149587407 | Common:1; Rare:29 | ||||
| chr2:149587672-149587818 | Common:1; Rare:42; Clinvar:1 | ||||
| chr2:151828459-151828598 | Common:1; Rare:35 | ||||
| chr2:152098703-152098953 | Common:1; Rare:63 | ||||
| chr2:152175659-152176063 | Common:2; Rare:120 | ||||
| chr2:152717829-152717972 | Rare:61 | ||||
| chr2:152717985-152718059 | Rare:24 |