| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:144517308-144517669 | Common:5; Rare:107; Clinvar:3; Clinvar (benign):5 | ||||
| chr2:144518134-144518203 | Common:1; Rare:14 | ||||
| chr2:144520063-144520498 | Common:4; Rare:87; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:144524431-144524604 | Common:4; Rare:49 | ||||
| chr2:148020673-148021397 | Common:2; Rare:170; Clinvar (benign):2 | ||||
| chr2:148021399-148021477 | Rare:18 | ||||
| chr2:148021528-148021658 | Rare:25 | ||||
| chr2:148068419-148068574 | Rare:24 | ||||
| chr2:148645378-148645439 | Rare:23 | ||||
| chr2:148875584-148875648 | Rare:21; Clinvar (benign):1 | ||||
| chr2:148947729-148947934 | Rare:54 | ||||
| chr2:149038661-149038783 | Common:1; Rare:49 | ||||
| chr2:149118029-149118211 | Common:1; Rare:30 | ||||
| chr2:149330330-149330609 | Common:1; Rare:119 | ||||
| chr2:149367571-149367730 | Common:1; Rare:25 |