| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:77800273-77800613 | Common:1; Rare:61 | ||||
| chr14:79279167-79279385 | Common:3; Rare:49 | ||||
| chr14:80941635-80941993 | Common:5; Rare:88 | ||||
| chr14:81219878-81220449 | Common:4; Rare:151 | ||||
| chr14:81220783-81221647 | Common:4; Rare:294 | ||||
| chr14:81221776-81221857 | Rare:23 | ||||
| chr14:81324049-81324373 | Common:1; Rare:54 | ||||
| chr14:81436406-81436643 | Common:4; Rare:90 | ||||
| chr14:81533592-81533677 | Rare:36 | ||||
| chr14:81533736-81534220 | Common:1; Rare:139 | ||||
| chr14:85529825-85530172 | Common:2; Rare:72 | ||||
| chr14:87993148-87993296 | Rare:60; Clinvar:6; Clinvar (pathogenic):2 | ||||
| chr14:88385497-88385770 | Common:2; Rare:84; Clinvar:2 | ||||
| chr14:88385906-88385986 | Common:4; Rare:21 | ||||
| chr14:88551320-88551642 | Common:3; Rare:80 |