| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24299749-24299890 | Common:1; Rare:46 | ||||
| chr14:24442644-24443043 | Common:6; Rare:124 | ||||
| chr14:30559055-30559221 | Common:2; Rare:64 | ||||
| chr14:30622190-30622381 | Common:1; Rare:92 | ||||
| chr14:31207639-31207862 | Common:2; Rare:80 | ||||
| chr14:31420526-31420763 | Common:3; Rare:71 | ||||
| chr14:31561349-31561456 | Common:1; Rare:40; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr14:32076694-32077045 | Common:3; Rare:108 | ||||
| chr14:34462214-34462548 | Common:1; Rare:114 | ||||
| chr14:34875299-34875472 | Rare:68 | ||||
| chr14:34982373-34982719 | Common:1; Rare:141 | ||||
| chr14:35046119-35046535 | Common:2; Rare:142 | ||||
| chr14:35121945-35122772 | Common:4; Rare:234 | ||||
| chr14:35292179-35292491 | Common:5; Rare:111; Clinvar:1 | ||||
| chr14:35826734-35826935 | Common:1; Rare:54 |