| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:22538965-22539080 | Rare:21 | ||||
| chr14:22547356-22547649 | Common:2; Rare:83 | ||||
| chr14:22551732-22551866 | Common:5; Rare:40 | ||||
| chr14:22770904-22771085 | Rare:55 | ||||
| chr14:22773662-22773865 | Common:1; Rare:61; Clinvar (pathogenic):1 | ||||
| chr14:24006763-24007094 | Common:2; Rare:84 | ||||
| chr14:24436209-24436463 | Common:2; Rare:57 | ||||
| chr14:31123019-31123066 | Rare:9 | ||||
| chr14:31876906-31877210 | Common:2; Rare:49 | ||||
| chr14:32203260-32203583 | Common:13; Rare:141 | ||||
| chr14:34780226-34780411 | Rare:36 | ||||
| chr14:34873776-34873842 | Common:1; Rare:18 | ||||
| chr14:34873873-34874231 | Common:3; Rare:76 | ||||
| chr14:35339935-35340099 | Common:1; Rare:29 | ||||
| chr14:39421484-39421664 | Rare:37 |