| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:23953661-23953797 | Common:5; Rare:49 | ||||
| chr14:24094004-24094319 | Common:3; Rare:86 | ||||
| chr14:24114921-24115325 | Common:2; Rare:115 | ||||
| chr14:24146549-24146744 | Rare:70 | ||||
| chr14:24195380-24195746 | Common:2; Rare:84 | ||||
| chr14:24213062-24213188 | Rare:24 | ||||
| chr14:24213408-24213592 | Common:1; Rare:65 | ||||
| chr14:24232312-24232707 | Common:8; Rare:93 | ||||
| chr14:24232832-24232949 | Rare:25 | ||||
| chr14:24242562-24242749 | Common:1; Rare:39; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:24271453-24271630 | Common:1; Rare:51 | ||||
| chr14:24299691-24299907 | Common:4; Rare:72 | ||||
| chr14:24429852-24429976 | Rare:31 | ||||
| chr14:24442702-24443056 | Common:5; Rare:107 | ||||
| chr14:30559049-30559216 | Common:2; Rare:65 |