| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:91510233-91510631 | Common:1; Rare:129 | ||||
| chr14:91836421-91836717 | Common:12; Rare:54 | ||||
| chr14:92040004-92040192 | Common:3; Rare:58; Clinvar:3; Clinvar (benign):2 | ||||
| chr14:92106532-92106717 | Common:2; Rare:59 | ||||
| chr14:92121649-92122005 | Common:5; Rare:123 | ||||
| chr14:92748519-92748769 | Rare:61 | ||||
| chr14:93115179-93115577 | Common:3; Rare:136 | ||||
| chr14:93184817-93185270 | Rare:144 | ||||
| chr14:93206964-93207327 | Common:3; Rare:181 | ||||
| chr14:93976527-93976803 | Rare:54 | ||||
| chr14:94081123-94081376 | Common:5; Rare:81 | ||||
| chr14:94129558-94129736 | Common:3; Rare:62 | ||||
| chr14:94390597-94390768 | Common:1; Rare:47 | ||||
| chr14:95157411-95157716 | Common:4; Rare:109 | ||||
| chr14:95534568-95534672 | Rare:44 |