| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:91510264-91510415 | Rare:51 | ||||
| chr14:91510457-91510572 | Common:1; Rare:33 | ||||
| chr14:91836421-91836706 | Common:12; Rare:52 | ||||
| chr14:91946964-91947136 | Common:1; Rare:23 | ||||
| chr14:92039826-92039979 | Rare:29; Clinvar:3 | ||||
| chr14:92040019-92040124 | Common:2; Rare:35; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:92106554-92106759 | Common:2; Rare:67 | ||||
| chr14:92121640-92122005 | Common:5; Rare:126 | ||||
| chr14:92748602-92748827 | Rare:61 | ||||
| chr14:92793988-92794408 | Rare:135 | ||||
| chr14:93184834-93185005 | Rare:56 | ||||
| chr14:93206982-93207288 | Common:2; Rare:148 | ||||
| chr14:93976719-93976839 | Rare:21 | ||||
| chr14:94081130-94081387 | Common:5; Rare:79 | ||||
| chr14:95157422-95157711 | Common:4; Rare:102 |