| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:47513672-47513833 | Rare:43 | ||||
| chr3:47781784-47782064 | Common:1; Rare:114 | ||||
| chr3:47802908-47803199 | Common:1; Rare:86 | ||||
| chr3:48088784-48089097 | Rare:106 | ||||
| chr3:48089270-48089361 | Rare:25 | ||||
| chr3:48301336-48301435 | Common:1; Rare:30 | ||||
| chr3:48440035-48440341 | Common:1; Rare:121 | ||||
| chr3:48504067-48504302 | Common:2; Rare:75 | ||||
| chr3:48556773-48557173 | Common:1; Rare:93 | ||||
| chr3:48635407-48635627 | Rare:73 | ||||
| chr3:48918702-48918920 | Common:2; Rare:110 | ||||
| chr3:49007180-49007426 | Common:2; Rare:95 | ||||
| chr3:49018538-49018634 | Rare:36 | ||||
| chr3:49021494-49021710 | Rare:54; Clinvar:1 | ||||
| chr3:49022081-49022179 | Rare:43; Clinvar (pathogenic):1 |