| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:47163900-47164220 | Common:1; Rare:89; Clinvar (pathogenic):1 | ||||
| chr3:47380806-47381073 | Rare:86 | ||||
| chr3:47381436-47381548 | Rare:24 | ||||
| chr3:47475801-47476084 | Common:3; Rare:110 | ||||
| chr3:47513644-47513767 | Common:1; Rare:43 | ||||
| chr3:47802929-47803203 | Common:1; Rare:84 | ||||
| chr3:48088784-48089057 | Rare:87 | ||||
| chr3:48241050-48241191 | Common:2; Rare:53 | ||||
| chr3:48301319-48301449 | Common:1; Rare:41 | ||||
| chr3:48429993-48430242 | Common:1; Rare:61 | ||||
| chr3:48440027-48440341 | Common:1; Rare:125 | ||||
| chr3:48556789-48557173 | Common:1; Rare:86 | ||||
| chr3:48918752-48918930 | Common:2; Rare:106 | ||||
| chr3:49007205-49007451 | Common:2; Rare:102 | ||||
| chr3:49029372-49029546 | Common:2; Rare:118 |