| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:48504090-48504298 | Common:2; Rare:69 | ||||
| chr3:48847663-48847946 | Common:1; Rare:75 | ||||
| chr3:48918791-48918889 | Common:2; Rare:56 | ||||
| chr3:49021503-49021703 | Rare:51; Clinvar:1 | ||||
| chr3:49029346-49029467 | Common:1; Rare:86 | ||||
| chr3:49094023-49094292 | Rare:62 | ||||
| chr3:49104720-49105052 | Rare:122; Clinvar:1; Clinvar (benign):4 | ||||
| chr3:49339984-49340146 | Common:2; Rare:70 | ||||
| chr3:49358256-49358497 | Common:3; Rare:129 | ||||
| chr3:49411820-49412213 | Common:1; Rare:125 | ||||
| chr3:49429223-49429461 | Common:1; Rare:56 | ||||
| chr3:49470002-49470328 | Common:2; Rare:98 | ||||
| chr3:49674225-49674402 | Common:1; Rare:70 | ||||
| chr3:49689460-49689597 | Rare:42 | ||||
| chr3:49723904-49724063 | Common:3; Rare:62 |