| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:77306441-77306659 | Common:2; Rare:37; Clinvar (benign):1 | ||||
| chr14:77306681-77307259 | Common:2; Rare:124 | ||||
| chr14:77320231-77320494 | Common:3; Rare:84; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr14:77320867-77321104 | Rare:72; Clinvar:1 | ||||
| chr14:77321200-77321490 | Common:4; Rare:153 | ||||
| chr14:77377045-77377213 | Common:1; Rare:57 | ||||
| chr14:77377279-77377455 | Common:1; Rare:60 | ||||
| chr14:77457516-77457833 | Common:1; Rare:105 | ||||
| chr14:77458007-77458138 | Rare:36 | ||||
| chr14:77458511-77458680 | Common:1; Rare:33 | ||||
| chr14:77616604-77617105 | Common:3; Rare:131; Clinvar:3; Clinvar (benign):5 | ||||
| chr14:77707981-77708218 | Common:2; Rare:119 | ||||
| chr14:77760440-77760810 | Common:4; Rare:116 | ||||
| chr14:77761091-77761279 | Common:1; Rare:70 | ||||
| chr14:77799968-77800140 | Rare:33 |