| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:39432420-39432662 | Common:6; Rare:81 | ||||
| chr14:44961892-44962258 | Common:3; Rare:106 | ||||
| chr14:45253059-45253319 | Rare:74 | ||||
| chr14:49586327-49586770 | Common:1; Rare:237; Clinvar (benign):1 | ||||
| chr14:49598731-49599032 | Common:1; Rare:108 | ||||
| chr14:49620570-49620835 | Common:2; Rare:110; Clinvar:3 | ||||
| chr14:49688199-49688272 | Rare:27 | ||||
| chr14:49892897-49893136 | Rare:102 | ||||
| chr14:50116548-50116696 | Rare:69 | ||||
| chr14:50312146-50312374 | Rare:99 | ||||
| chr14:50396863-50396991 | Common:1; Rare:33 | ||||
| chr14:50532460-50532787 | Common:4; Rare:104 | ||||
| chr14:50668322-50668556 | Common:3; Rare:86 | ||||
| chr14:50944287-50944620 | Common:5; Rare:118; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr14:51240145-51240311 | Rare:77 |