| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:127598219-127598458 | Common:3; Rare:71 | ||||
| chr3:127628940-127629227 | Common:1; Rare:96 | ||||
| chr3:127822451-127822671 | Rare:48 | ||||
| chr3:127823180-127823375 | Common:3; Rare:40 | ||||
| chr3:128052166-128052495 | Common:2; Rare:109 | ||||
| chr3:128123729-128124013 | Rare:85 | ||||
| chr3:128879421-128879675 | Common:4; Rare:124; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:129183807-129184079 | Common:2; Rare:90 | ||||
| chr3:129249503-129249680 | Common:3; Rare:53 | ||||
| chr3:129278761-129278882 | Common:4; Rare:40 | ||||
| chr3:129316227-129316340 | Rare:58 | ||||
| chr3:129439861-129440254 | Common:1; Rare:115; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:129893552-129893882 | Rare:132 | ||||
| chr3:130746796-130746947 | Common:3; Rare:44 | ||||
| chr3:131026727-131026940 | Common:2; Rare:55 |