| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:48918787-48918895 | Common:2; Rare:62 | ||||
| chr3:49007135-49007426 | Common:2; Rare:117 | ||||
| chr3:49021502-49021710 | Rare:52; Clinvar:1 | ||||
| chr3:49029372-49029535 | Common:2; Rare:112 | ||||
| chr3:49104720-49104910 | Rare:82; Clinvar:1; Clinvar (benign):4 | ||||
| chr3:49120754-49120997 | Rare:74 | ||||
| chr3:49122337-49122508 | Rare:29 | ||||
| chr3:49132969-49133161 | Rare:40; Clinvar:2 | ||||
| chr3:49166289-49166449 | Common:1; Rare:41 | ||||
| chr3:49171476-49171642 | Common:2; Rare:37 | ||||
| chr3:49411874-49412429 | Common:2; Rare:202 | ||||
| chr3:49429250-49429438 | Rare:47 | ||||
| chr3:49470004-49470325 | Common:1; Rare:96 | ||||
| chr3:49674225-49674402 | Common:1; Rare:70 | ||||
| chr3:49689460-49689613 | Rare:47 |