| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:22956980-22957193 | Rare:60 | ||||
| chr14:22982509-22982967 | Common:3; Rare:158 | ||||
| chr14:23007138-23007320 | Common:2; Rare:47 | ||||
| chr14:23010112-23010268 | Rare:49 | ||||
| chr14:23034859-23035209 | Common:2; Rare:75 | ||||
| chr14:23071546-23071642 | Rare:26 | ||||
| chr14:23094429-23094760 | Common:2; Rare:104 | ||||
| chr14:23095099-23095616 | Common:3; Rare:225 | ||||
| chr14:23154391-23154508 | Common:3; Rare:35 | ||||
| chr14:23286042-23286400 | Common:2; Rare:96 | ||||
| chr14:23302811-23302967 | Rare:30 | ||||
| chr14:23306645-23306890 | Common:1; Rare:51 | ||||
| chr14:23321549-23321814 | Common:2; Rare:83; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:23321817-23322074 | Common:2; Rare:75 | ||||
| chr14:23407389-23407816 | Common:1; Rare:68; Clinvar (benign):3 |