| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:91510268-91510637 | Common:1; Rare:119 | ||||
| chr14:92040013-92040198 | Common:3; Rare:59; Clinvar:3; Clinvar (benign):2 | ||||
| chr14:92121647-92121997 | Common:5; Rare:117 | ||||
| chr14:92748621-92748817 | Rare:51 | ||||
| chr14:92793995-92794366 | Rare:114 | ||||
| chr14:93184837-93185014 | Rare:61 | ||||
| chr14:93206985-93207306 | Common:2; Rare:159 | ||||
| chr14:93955286-93955387 | Common:2; Rare:18 | ||||
| chr14:94081141-94081341 | Common:4; Rare:67 | ||||
| chr14:94129575-94129701 | Common:3; Rare:42 | ||||
| chr14:95157430-95157697 | Common:4; Rare:96 | ||||
| chr14:95534464-95534710 | Common:3; Rare:90 | ||||
| chr14:95686230-95686443 | Common:1; Rare:59 | ||||
| chr14:95714054-95714259 | Common:1; Rare:75 | ||||
| chr14:96363283-96363552 | Common:1; Rare:90 |