| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:23096322-23096359 | Rare:5 | ||||
| chr14:23120155-23120175 | |||||
| chr14:23120866-23121043 | Rare:40 | ||||
| chr14:23285295-23285439 | Common:1; Rare:21 | ||||
| chr14:23447769-23448040 | Common:1; Rare:40 | ||||
| chr14:23606193-23606459 | Rare:37 | ||||
| chr14:24006924-24007119 | Common:2; Rare:57 | ||||
| chr14:24036271-24036535 | Common:4; Rare:104 | ||||
| chr14:24036800-24036940 | Common:2; Rare:41 | ||||
| chr14:24081078-24081316 | Common:1; Rare:74; Clinvar:3; Clinvar (benign):1 | ||||
| chr14:24108904-24109143 | Rare:39 | ||||
| chr14:24140720-24140937 | Rare:62 | ||||
| chr14:24196538-24196638 | Rare:14 | ||||
| chr14:24233479-24233738 | Common:3; Rare:89 | ||||
| chr14:24246960-24247107 | Rare:30 |