| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:29927813-29927961 | Common:1; Rare:50 | ||||
| chr14:30622190-30622405 | Common:1; Rare:100 | ||||
| chr14:31025557-31025678 | Common:1; Rare:31 | ||||
| chr14:31025910-31026077 | Common:1; Rare:53 | ||||
| chr14:31026162-31026270 | Rare:28 | ||||
| chr14:31026359-31026638 | Common:4; Rare:86 | ||||
| chr14:31112504-31112820 | Common:3; Rare:74 | ||||
| chr14:31207409-31207869 | Common:2; Rare:146 | ||||
| chr14:31420481-31420763 | Common:4; Rare:94 | ||||
| chr14:31457036-31457209 | Rare:41 | ||||
| chr14:31561328-31561570 | Common:2; Rare:85; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr14:32076664-32077056 | Common:3; Rare:117 | ||||
| chr14:34461897-34462146 | Common:1; Rare:62 | ||||
| chr14:34462226-34462551 | Common:1; Rare:109 | ||||
| chr14:34629909-34630252 | Common:5; Rare:135 |