| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:48440035-48440324 | Common:1; Rare:110 | ||||
| chr3:48446622-48446746 | Common:1; Rare:43 | ||||
| chr3:48504048-48504323 | Common:2; Rare:86 | ||||
| chr3:48556789-48557149 | Common:1; Rare:81 | ||||
| chr3:48635410-48635608 | Rare:66 | ||||
| chr3:48695392-48695449 | Common:1; Rare:4 | ||||
| chr3:48847648-48847962 | Common:1; Rare:84 | ||||
| chr3:48918703-48918964 | Common:2; Rare:136 | ||||
| chr3:48989731-48989926 | Rare:52 | ||||
| chr3:49007166-49007457 | Common:2; Rare:121 | ||||
| chr3:49018549-49018625 | Rare:26 | ||||
| chr3:49021502-49021738 | Rare:56; Clinvar:1 | ||||
| chr3:49022009-49022185 | Rare:61; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr3:49029291-49029557 | Common:2; Rare:167 | ||||
| chr3:49094313-49094637 | Common:2; Rare:80 |