| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24146564-24146882 | Common:1; Rare:100 | ||||
| chr14:24195410-24195781 | Common:1; Rare:89 | ||||
| chr14:24213083-24213191 | Rare:21 | ||||
| chr14:24213440-24213592 | Common:1; Rare:52 | ||||
| chr14:24215958-24216037 | Common:1; Rare:31 | ||||
| chr14:24216047-24216122 | Rare:20 | ||||
| chr14:24232305-24232673 | Common:8; Rare:92 | ||||
| chr14:24232826-24232929 | Rare:24 | ||||
| chr14:24242580-24242774 | Common:1; Rare:47; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:24271460-24271609 | Common:1; Rare:44 | ||||
| chr14:24299722-24299869 | Common:4; Rare:42 | ||||
| chr14:24429855-24429970 | Rare:25 | ||||
| chr14:24442663-24443013 | Common:5; Rare:114 | ||||
| chr14:30559049-30559221 | Common:2; Rare:67 | ||||
| chr14:30622194-30622350 | Rare:56 |