| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:57555936-57556394 | Rare:135 | ||||
| chr3:57597266-57597941 | Common:7; Rare:208 | ||||
| chr3:57598620-57598709 | Rare:22 | ||||
| chr3:57692526-57692893 | Common:3; Rare:109 | ||||
| chr3:57692983-57693252 | Common:2; Rare:81 | ||||
| chr3:57755824-57755888 | Rare:14 | ||||
| chr3:57756075-57756364 | Rare:74 | ||||
| chr3:58008215-58008538 | Common:2; Rare:113; Clinvar:5; Clinvar (benign):1 | ||||
| chr3:58214683-58214853 | Rare:29 | ||||
| chr3:58214997-58215276 | Common:2; Rare:67 | ||||
| chr3:58237355-58237817 | Common:11; Rare:125 | ||||
| chr3:58306115-58306377 | Common:1; Rare:73 | ||||
| chr3:58306450-58306627 | Common:3; Rare:66 | ||||
| chr3:58332702-58332963 | Common:10; Rare:66 | ||||
| chr3:58333648-58333708 | Rare:14 |