| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:91509982-91510079 | Common:1; Rare:31 | ||||
| chr14:91510083-91510130 | Rare:13 | ||||
| chr14:91510158-91510737 | Common:2; Rare:207 | ||||
| chr14:91510754-91510935 | Common:1; Rare:47 | ||||
| chr14:91511031-91511096 | Common:1; Rare:13 | ||||
| chr14:91836439-91836808 | Common:13; Rare:72 | ||||
| chr14:91947336-91947352 | Rare:1 | ||||
| chr14:91947578-91947814 | Common:2; Rare:73; Clinvar:3; Clinvar (benign):4 | ||||
| chr14:92039389-92039702 | Common:2; Rare:92; Clinvar (benign):2 | ||||
| chr14:92039787-92039835 | Rare:7; Clinvar:1 | ||||
| chr14:92039969-92040288 | Common:4; Rare:86; Clinvar:3; Clinvar (benign):2 | ||||
| chr14:92040347-92040513 | Common:1; Rare:23 | ||||
| chr14:92040707-92041039 | Common:3; Rare:56 | ||||
| chr14:92106062-92106412 | Common:1; Rare:104 | ||||
| chr14:92106486-92106878 | Common:3; Rare:119 |