| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:23321878-23322009 | Common:1; Rare:37 | ||||
| chr14:23556222-23556278 | Rare:10 | ||||
| chr14:23567761-23567873 | Rare:24 | ||||
| chr14:23953638-23953810 | Common:7; Rare:65 | ||||
| chr14:24094027-24094348 | Common:3; Rare:79 | ||||
| chr14:24141501-24141809 | Common:2; Rare:75 | ||||
| chr14:24146543-24146752 | Rare:74 | ||||
| chr14:24195420-24195709 | Common:1; Rare:67 | ||||
| chr14:24232312-24232706 | Common:8; Rare:93 | ||||
| chr14:24232823-24232949 | Common:1; Rare:26 | ||||
| chr14:24242586-24242774 | Common:1; Rare:45; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:24271520-24271650 | Common:1; Rare:32 | ||||
| chr14:24299749-24299890 | Common:1; Rare:46 | ||||
| chr14:24442681-24443023 | Common:5; Rare:109 | ||||
| chr14:30559055-30559191 | Common:2; Rare:47 |