| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:23306701-23307028 | Common:1; Rare:69 | ||||
| chr14:23308433-23308683 | Rare:37 | ||||
| chr14:23321145-23321819 | Common:4; Rare:210; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr14:23322523-23322749 | Common:1; Rare:46 | ||||
| chr14:23365092-23365325 | Rare:59 | ||||
| chr14:23548385-23548544 | Rare:41 | ||||
| chr14:23551735-23551856 | Rare:25 | ||||
| chr14:23555895-23556390 | Common:4; Rare:118 | ||||
| chr14:23567468-23567579 | Rare:32 | ||||
| chr14:23567737-23567822 | Rare:19 | ||||
| chr14:23567835-23567862 | Rare:1 | ||||
| chr14:23953622-23953885 | Common:10; Rare:107 | ||||
| chr14:23954116-23954272 | Common:2; Rare:49 | ||||
| chr14:23969847-23969970 | Common:7; Rare:55 | ||||
| chr14:23988751-23988848 | Common:6; Rare:37 |