| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:92040019-92040124 | Common:2; Rare:35; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:92121656-92121999 | Common:5; Rare:115 | ||||
| chr14:92513331-92513384 | Common:1; Rare:13 | ||||
| chr14:92513601-92513918 | Common:4; Rare:73 | ||||
| chr14:92748594-92748763 | Rare:45 | ||||
| chr14:93184829-93185013 | Rare:64 | ||||
| chr14:93206991-93207288 | Common:2; Rare:146 | ||||
| chr14:93976448-93976674 | Rare:49 | ||||
| chr14:93976694-93976878 | Rare:29 | ||||
| chr14:94081123-94081383 | Common:5; Rare:83 | ||||
| chr14:94390553-94390827 | Common:2; Rare:67 | ||||
| chr14:95157246-95157707 | Common:5; Rare:149; Clinvar:2; Clinvar (benign):2 | ||||
| chr14:95534609-95534657 | Rare:11 | ||||
| chr14:95534771-95535002 | Common:3; Rare:63 | ||||
| chr14:95535348-95535381 | Rare:15 |