| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:77040148-77040616 | Rare:121 | ||||
| chr14:77042091-77042401 | Common:3; Rare:39 | ||||
| chr14:77045610-77046020 | Common:20; Rare:193 | ||||
| chr14:77087758-77087899 | Common:1; Rare:24 | ||||
| chr14:77088206-77088631 | Common:4; Rare:169 | ||||
| chr14:77111140-77111506 | Rare:114 | ||||
| chr14:77184380-77184690 | Common:1; Rare:65 | ||||
| chr14:77184798-77185217 | Common:11; Rare:174 | ||||
| chr14:77204400-77204708 | Rare:59 | ||||
| chr14:77302930-77303569 | Common:2; Rare:121; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr14:77303692-77303990 | Rare:41 | ||||
| chr14:77311360-77311680 | Rare:48 | ||||
| chr14:77400125-77400624 | Common:1; Rare:109 | ||||
| chr14:77590691-77591595 | Common:9; Rare:292 | ||||
| chr14:77864148-77864385 | Common:3; Rare:41 |