| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:53800119-53800388 | Common:1; Rare:65; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:53842950-53843128 | Common:1; Rare:28 | ||||
| chr3:53845530-53845872 | Common:1; Rare:120 | ||||
| chr3:53857313-53857592 | Common:2; Rare:50 | ||||
| chr3:53927453-53927853 | Common:9; Rare:263 | ||||
| chr3:54064586-54064986 | Common:7; Rare:116 | ||||
| chr3:54353887-54354104 | Common:2; Rare:33 | ||||
| chr3:54891480-54891948 | Common:4; Rare:217 | ||||
| chr3:55571918-55572375 | Common:9; Rare:229 | ||||
| chr3:56061240-56061560 | Common:1; Rare:65 | ||||
| chr3:56811110-56811840 | Common:4; Rare:119 | ||||
| chr3:57004152-57004452 | Common:4; Rare:57 | ||||
| chr3:57006456-57006744 | Common:1; Rare:56 | ||||
| chr3:57039420-57040100 | Common:5; Rare:114 | ||||
| chr3:57109518-57109783 | Rare:73 |