| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:28308840-28309058 | Common:11; Rare:59 | ||||
| chr3:29757525-29757675 | Common:1; Rare:24 | ||||
| chr3:30611990-30612158 | Common:1; Rare:27 | ||||
| chr3:30622937-30623217 | Rare:54; Clinvar (benign):2 | ||||
| chr3:30631496-30631611 | Rare:15 | ||||
| chr3:30652974-30653112 | Rare:18 | ||||
| chr3:30669782-30669964 | Common:4; Rare:26 | ||||
| chr3:30681289-30681669 | Common:2; Rare:65 | ||||
| chr3:30696891-30697151 | Common:2; Rare:53 | ||||
| chr3:30703517-30703742 | Common:1; Rare:35 | ||||
| chr3:30709404-30709453 | Rare:7 | ||||
| chr3:30711332-30711402 | Rare:13 | ||||
| chr3:30715071-30715105 | Rare:5 | ||||
| chr3:30942921-30943068 | Common:1; Rare:33 | ||||
| chr3:31579512-31579842 | Common:4; Rare:58 |