| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31508010-31508112 | Rare:32 | ||||
| chr16:31508296-31508535 | Common:4; Rare:108 | ||||
| chr16:31713112-31713359 | Common:1; Rare:59 | ||||
| chr16:31713526-31713600 | Rare:23 | ||||
| chr16:31713625-31713680 | Rare:11 | ||||
| chr16:31713766-31713884 | Rare:22 | ||||
| chr16:31873604-31873957 | Common:1; Rare:111 | ||||
| chr16:31874087-31874169 | Rare:13 | ||||
| chr16:46621312-46621496 | Rare:75 | ||||
| chr16:46688594-46688812 | Rare:51 | ||||
| chr16:46689111-46689404 | Common:1; Rare:107; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46689501-46689742 | Common:2; Rare:106; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:46689850-46689967 | Rare:28 | ||||
| chr16:46690105-46690282 | Rare:40 | ||||
| chr16:46748296-46748614 | Rare:58 |