| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:22836505-22836686 | Common:2; Rare:36 | ||||
| chr14:22871513-22871874 | Rare:84 | ||||
| chr14:22872024-22872175 | Common:2; Rare:31 | ||||
| chr14:22929332-22929639 | Common:1; Rare:87 | ||||
| chr14:22982553-22982956 | Common:3; Rare:139 | ||||
| chr14:23010117-23010245 | Rare:40 | ||||
| chr14:23034854-23035225 | Common:2; Rare:78 | ||||
| chr14:23071554-23071666 | Rare:32 | ||||
| chr14:23095042-23095594 | Common:3; Rare:236 | ||||
| chr14:23154319-23154680 | Common:5; Rare:79 | ||||
| chr14:23286046-23286283 | Rare:74 | ||||
| chr14:23306479-23306890 | Common:1; Rare:85 | ||||
| chr14:23376695-23377051 | Rare:60 | ||||
| chr14:23407549-23407820 | Rare:45; Clinvar (benign):3 | ||||
| chr14:23435545-23435991 | Common:2; Rare:92; Clinvar (benign):1 |