| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:74963260-74963540 | Common:2; Rare:58 | ||||
| chr14:75008725-75009240 | Common:4; Rare:278; Clinvar:10; Clinvar (benign):1; Clinvar (pathogenic):8 | ||||
| chr14:75011444-75012010 | Common:2; Rare:130 | ||||
| chr14:75012009-75012492 | Common:8; Rare:129 | ||||
| chr14:75068217-75068617 | Common:3; Rare:104 | ||||
| chr14:75124023-75124423 | Common:3; Rare:136 | ||||
| chr14:75126115-75126336 | Rare:88 | ||||
| chr14:75222150-75222760 | Common:4; Rare:142 | ||||
| chr14:75258932-75259390 | Common:4; Rare:207 | ||||
| chr14:75294140-75294510 | Common:3; Rare:154 | ||||
| chr14:75295883-75296545 | Common:9; Rare:173 | ||||
| chr14:75334195-75334419 | Common:1; Rare:50 | ||||
| chr14:75334594-75334799 | Common:1; Rare:46 | ||||
| chr14:75335710-75335968 | Common:3; Rare:59 | ||||
| chr14:75341014-75341733 | Common:4; Rare:134 |