| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:23555941-23556059 | Rare:33 | ||||
| chr14:23567742-23567843 | Rare:23 | ||||
| chr14:23953638-23953810 | Common:7; Rare:65 | ||||
| chr14:23988762-23988929 | Common:8; Rare:67 | ||||
| chr14:24114478-24114843 | Common:1; Rare:88 | ||||
| chr14:24114921-24115319 | Common:2; Rare:113 | ||||
| chr14:24141486-24141733 | Common:2; Rare:64 | ||||
| chr14:24146577-24146697 | Rare:44 | ||||
| chr14:24195410-24195744 | Common:1; Rare:75 | ||||
| chr14:24213062-24213182 | Rare:21 | ||||
| chr14:24232274-24232742 | Common:8; Rare:118 | ||||
| chr14:24232747-24232952 | Common:1; Rare:44 | ||||
| chr14:24242247-24242429 | Common:1; Rare:57; Clinvar:1; Clinvar (benign):3 | ||||
| chr14:24299738-24299879 | Common:4; Rare:40 | ||||
| chr14:24367916-24368216 | Common:2; Rare:49 |