| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24429855-24429974 | Rare:28 | ||||
| chr14:24430093-24430317 | Common:3; Rare:64 | ||||
| chr14:24442650-24443017 | Common:5; Rare:119 | ||||
| chr14:26597433-26597681 | Common:1; Rare:45 | ||||
| chr14:30559094-30559227 | Common:1; Rare:50 | ||||
| chr14:31025344-31025664 | Common:2; Rare:72 | ||||
| chr14:31207596-31207862 | Common:2; Rare:94 | ||||
| chr14:31420524-31420875 | Common:4; Rare:97 | ||||
| chr14:31561089-31561515 | Common:4; Rare:121; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr14:32076074-32076308 | Common:2; Rare:59 | ||||
| chr14:32076691-32077045 | Common:3; Rare:108 | ||||
| chr14:33951052-33951267 | Common:1; Rare:68 | ||||
| chr14:34462188-34462558 | Common:1; Rare:134 | ||||
| chr14:34539619-34539804 | Rare:63 | ||||
| chr14:34714536-34714781 | Common:3; Rare:90 |