| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:48089221-48089363 | Rare:45 | ||||
| chr3:48301325-48301449 | Common:1; Rare:39 | ||||
| chr3:48440027-48440341 | Common:1; Rare:125 | ||||
| chr3:48504090-48504302 | Common:2; Rare:69 | ||||
| chr3:48847663-48847957 | Common:1; Rare:80 | ||||
| chr3:48918724-48918959 | Common:2; Rare:129 | ||||
| chr3:49007177-49007464 | Common:2; Rare:115 | ||||
| chr3:49021503-49021721 | Rare:55; Clinvar:1 | ||||
| chr3:49021993-49022183 | Rare:66; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr3:49104604-49104870 | Common:1; Rare:113; Clinvar:5; Clinvar (benign):7 | ||||
| chr3:49120747-49121116 | Rare:103 | ||||
| chr3:49132924-49133148 | Rare:42; Clinvar:2 | ||||
| chr3:49340003-49340110 | Common:2; Rare:52 | ||||
| chr3:49358025-49358525 | Common:4; Rare:248 | ||||
| chr3:49411839-49412429 | Common:2; Rare:210 |