| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:91244590-91244950 | Common:3; Rare:68 | ||||
| chr14:91417570-91417674 | Common:1; Rare:34; Clinvar (benign):1 | ||||
| chr14:91510068-91510393 | Rare:115 | ||||
| chr14:91510497-91510832 | Common:2; Rare:106 | ||||
| chr14:91947570-91948000 | Common:5; Rare:108; Clinvar:3; Clinvar (benign):4 | ||||
| chr14:92039471-92039594 | Common:2; Rare:38; Clinvar (benign):2 | ||||
| chr14:92039973-92040229 | Common:3; Rare:77; Clinvar:3; Clinvar (benign):2 | ||||
| chr14:92106239-92106360 | Common:1; Rare:44 | ||||
| chr14:92106554-92106849 | Common:3; Rare:88 | ||||
| chr14:92121606-92122012 | Common:5; Rare:142 | ||||
| chr14:92122356-92122530 | Common:1; Rare:48 | ||||
| chr14:92449888-92450010 | Common:1; Rare:24 | ||||
| chr14:92513480-92513880 | Common:3; Rare:86 | ||||
| chr14:92748581-92748819 | Rare:66 | ||||
| chr14:92793918-92794425 | Rare:167 |