| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49021502-49021710 | Rare:52; Clinvar:1 | ||||
| chr3:49029365-49029498 | Common:1; Rare:98 | ||||
| chr3:49104616-49104947 | Common:1; Rare:130; Clinvar:3; Clinvar (benign):7 | ||||
| chr3:49132945-49133161 | Rare:40; Clinvar:2 | ||||
| chr3:49166294-49166437 | Common:1; Rare:35 | ||||
| chr3:49339998-49340132 | Common:2; Rare:62 | ||||
| chr3:49411839-49412440 | Common:2; Rare:214 | ||||
| chr3:49469971-49470325 | Common:1; Rare:113 | ||||
| chr3:49674218-49674537 | Common:1; Rare:117 | ||||
| chr3:49688664-49688678 | Rare:2 | ||||
| chr3:49689460-49689605 | Rare:45 | ||||
| chr3:49723879-49723993 | Common:2; Rare:39 | ||||
| chr3:49803148-49803287 | Rare:50 | ||||
| chr3:49810781-49811095 | Common:1; Rare:89 | ||||
| chr3:49812502-49812795 | Common:1; Rare:72 |