| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:21456042-21456254 | Common:4; Rare:58 | ||||
| chr14:21476870-21477281 | Common:2; Rare:135 | ||||
| chr14:21511267-21511553 | Rare:78 | ||||
| chr14:22589005-22589457 | Common:4; Rare:137 | ||||
| chr14:22766558-22766749 | Common:1; Rare:111 | ||||
| chr14:22929348-22929609 | Rare:61 | ||||
| chr14:23094483-23094760 | Common:2; Rare:94 | ||||
| chr14:23095105-23095576 | Common:3; Rare:212 | ||||
| chr14:23154291-23154578 | Common:4; Rare:67 | ||||
| chr14:23407026-23407387 | Common:2; Rare:95; Clinvar:10; Clinvar (benign):9 | ||||
| chr14:23555933-23556069 | Rare:36 | ||||
| chr14:23556230-23556348 | Common:1; Rare:24 | ||||
| chr14:23953638-23953819 | Common:7; Rare:68 | ||||
| chr14:23988772-23988969 | Common:9; Rare:85 | ||||
| chr14:24114921-24115316 | Common:2; Rare:112 |