| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:46971869-46971951 | Rare:16 | ||||
| chr3:46974538-46974627 | Common:2; Rare:12 | ||||
| chr3:46987720-46987999 | Common:2; Rare:86 | ||||
| chr3:46988123-46988181 | Common:1; Rare:12 | ||||
| chr3:46990862-46990945 | Rare:16 | ||||
| chr3:47009290-47009626 | Common:5; Rare:130; Clinvar:5; Clinvar (benign):4 | ||||
| chr3:47164762-47164849 | Common:2; Rare:22 | ||||
| chr3:47165301-47165349 | Rare:6 | ||||
| chr3:47227766-47227947 | Rare:32 | ||||
| chr3:47291840-47292001 | Rare:35 | ||||
| chr3:47380359-47380380 | Rare:9 | ||||
| chr3:47741953-47742216 | Common:1; Rare:44 | ||||
| chr3:47777827-47778122 | Common:1; Rare:43 | ||||
| chr3:47780335-47780522 | Rare:36 | ||||
| chr3:47781062-47781286 | Common:1; Rare:47 |