| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:74611897-74611995 | Rare:39; Clinvar:3 | ||||
| chr14:74612165-74612208 | Common:1; Rare:2; Clinvar (benign):1 | ||||
| chr14:74612511-74612772 | Common:1; Rare:70 | ||||
| chr14:74713021-74713260 | Common:1; Rare:126 | ||||
| chr14:74763123-74763454 | Rare:97 | ||||
| chr14:74763545-74763648 | Rare:40 | ||||
| chr14:74881697-74882089 | Common:1; Rare:150 | ||||
| chr14:74882152-74882389 | Rare:81 | ||||
| chr14:74922642-74922887 | Common:2; Rare:62 | ||||
| chr14:74923184-74923368 | Common:1; Rare:56 | ||||
| chr14:74955550-74955780 | Common:1; Rare:54 | ||||
| chr14:75002497-75003121 | Common:1; Rare:188; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr14:75003254-75003439 | Rare:53; Clinvar (pathogenic):1 | ||||
| chr14:75003442-75003483 | Rare:3 | ||||
| chr14:75049653-75049996 | Common:1; Rare:65; Clinvar:2 |