| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:67279039-67279091 | Rare:8 | ||||
| chr16:67279259-67279589 | Common:1; Rare:87 | ||||
| chr16:67393480-67393672 | Common:1; Rare:44 | ||||
| chr16:67416389-67416543 | Common:2; Rare:48 | ||||
| chr16:67430603-67430671 | Rare:13 | ||||
| chr16:67430889-67431124 | Common:3; Rare:42 | ||||
| chr16:67431154-67431334 | Rare:43; Clinvar (pathogenic):1 | ||||
| chr16:67481080-67481443 | Common:2; Rare:132 | ||||
| chr16:67528698-67528850 | Rare:45 | ||||
| chr16:67561892-67562671 | Common:1; Rare:247 | ||||
| chr16:67562731-67563032 | Common:2; Rare:83 | ||||
| chr16:67660182-67660420 | Rare:145; Clinvar:3; Clinvar (benign):2 | ||||
| chr16:67660696-67660990 | Common:3; Rare:98 | ||||
| chr16:67661420-67661513 | Rare:21 | ||||
| chr16:67719273-67719553 | Common:1; Rare:78 |