| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:22819727-22819885 | Common:3; Rare:33; Clinvar (benign):1 | ||||
| chr14:22829765-22829966 | Common:1; Rare:72 | ||||
| chr14:22836500-22836813 | Common:3; Rare:79 | ||||
| chr14:22871651-22872278 | Common:2; Rare:157 | ||||
| chr14:22929341-22929609 | Rare:66 | ||||
| chr14:22957021-22957193 | Rare:50 | ||||
| chr14:22982513-22982699 | Rare:70 | ||||
| chr14:23095099-23095186 | Rare:43 | ||||
| chr14:23095440-23095594 | Common:2; Rare:59 | ||||
| chr14:23286062-23286369 | Rare:76 | ||||
| chr14:23321817-23322009 | Common:1; Rare:55 | ||||
| chr14:23567756-23567805 | Rare:13 | ||||
| chr14:23953637-23953810 | Common:7; Rare:66 | ||||
| chr14:24115011-24115280 | Common:2; Rare:76 | ||||
| chr14:24146543-24146744 | Rare:73 |