| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:74018665-74018975 | Common:3; Rare:69 | ||||
| chr14:74019050-74019470 | Common:4; Rare:135 | ||||
| chr14:74084334-74085024 | Common:10; Rare:209 | ||||
| chr14:74085193-74085513 | Common:4; Rare:47 | ||||
| chr14:74302484-74302703 | Common:2; Rare:51 | ||||
| chr14:74302850-74303149 | Common:3; Rare:125; Clinvar (benign):4 | ||||
| chr14:74493024-74493071 | Rare:5 | ||||
| chr14:74493205-74493458 | Common:1; Rare:72; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr14:74493462-74493844 | Common:3; Rare:142; Clinvar (benign):4 | ||||
| chr14:74612543-74612874 | Common:1; Rare:80 | ||||
| chr14:74712997-74713247 | Common:1; Rare:133 | ||||
| chr14:74763123-74763447 | Rare:97 | ||||
| chr14:74763541-74763599 | Rare:25 | ||||
| chr14:74881742-74882001 | Common:1; Rare:116 | ||||
| chr14:74882288-74882312 | Rare:8 |