| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:91113982-91114155 | Common:1; Rare:51 | ||||
| chr14:91114247-91114445 | Rare:38 | ||||
| chr14:91510183-91510335 | Rare:64 | ||||
| chr14:91510346-91510737 | Common:2; Rare:130 | ||||
| chr14:91836373-91836699 | Common:14; Rare:59 | ||||
| chr14:92040028-92040186 | Common:2; Rare:43; Clinvar (benign):1 | ||||
| chr14:92121649-92122257 | Common:5; Rare:192 | ||||
| chr14:92513737-92513800 | Rare:10 | ||||
| chr14:92793961-92794253 | Rare:85 | ||||
| chr14:93184801-93185378 | Rare:179 | ||||
| chr14:93206985-93207342 | Common:3; Rare:175 | ||||
| chr14:93332396-93332744 | Common:2; Rare:102 | ||||
| chr14:93333001-93333275 | Common:2; Rare:108 | ||||
| chr14:94081121-94081440 | Common:5; Rare:93 | ||||
| chr14:94112483-94112779 | Common:2; Rare:60 |