| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:74713078-74713207 | Rare:63 | ||||
| chr14:75126978-75127116 | Rare:53 | ||||
| chr14:75660861-75661330 | Common:4; Rare:108 | ||||
| chr14:77320776-77321093 | Common:2; Rare:96; Clinvar:3; Clinvar (benign):2 | ||||
| chr14:77377049-77377417 | Common:2; Rare:107 | ||||
| chr14:77457555-77458143 | Common:2; Rare:161 | ||||
| chr14:77707985-77708133 | Common:1; Rare:77 | ||||
| chr14:81220867-81221077 | Common:1; Rare:97 | ||||
| chr14:85530047-85530200 | Common:1; Rare:36 | ||||
| chr14:92121658-92121993 | Common:4; Rare:112 | ||||
| chr14:93184851-93185008 | Rare:50 | ||||
| chr14:93207121-93207301 | Common:2; Rare:84 | ||||
| chr14:94081154-94081390 | Common:3; Rare:76 | ||||
| chr14:95534776-95535026 | Common:3; Rare:67 | ||||
| chr14:96363308-96363550 | Common:1; Rare:81 |