| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49021503-49021710 | Rare:52; Clinvar:1 | ||||
| chr3:49022073-49022154 | Rare:35; Clinvar (pathogenic):1 | ||||
| chr3:49025218-49025522 | Common:1; Rare:68 | ||||
| chr3:49120754-49120987 | Rare:73 | ||||
| chr3:49132979-49133148 | Rare:37; Clinvar:1 | ||||
| chr3:49166289-49166437 | Common:1; Rare:38 | ||||
| chr3:49339994-49340103 | Common:1; Rare:57 | ||||
| chr3:49358201-49358522 | Common:4; Rare:163 | ||||
| chr3:49411839-49412213 | Common:1; Rare:124 | ||||
| chr3:49412320-49412424 | Rare:38 | ||||
| chr3:49429246-49429404 | Rare:38 | ||||
| chr3:49470004-49470325 | Common:1; Rare:96 | ||||
| chr3:49673800-49674008 | Common:5; Rare:36 | ||||
| chr3:49674225-49674395 | Common:1; Rare:64 | ||||
| chr3:49689460-49689605 | Rare:45 |