| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:77458016-77458137 | Rare:33 | ||||
| chr14:77707991-77708131 | Common:1; Rare:71 | ||||
| chr14:81220871-81221069 | Common:1; Rare:94 | ||||
| chr14:88562935-88563116 | Rare:86 | ||||
| chr14:89954654-89954970 | Rare:97 | ||||
| chr14:90256481-90256611 | Common:1; Rare:43 | ||||
| chr14:90396895-90397107 | Common:2; Rare:111 | ||||
| chr14:91244672-91244825 | Common:2; Rare:28 | ||||
| chr14:91510285-91510637 | Common:1; Rare:111 | ||||
| chr14:92040019-92040177 | Common:2; Rare:49; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:92121658-92121990 | Common:4; Rare:109 | ||||
| chr14:93184856-93185013 | Rare:51 | ||||
| chr14:93206972-93207288 | Common:2; Rare:153 | ||||
| chr14:94081150-94081341 | Common:3; Rare:65 | ||||
| chr14:95534550-95534672 | Common:1; Rare:52 |