| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:3400965-3401254 | Common:6; Rare:107 | ||||
| chr16:3611572-3611731 | Rare:64 | ||||
| chr16:3717507-3717630 | Rare:64 | ||||
| chr16:4476317-4476473 | Rare:62 | ||||
| chr16:4734231-4734534 | Rare:95 | ||||
| chr16:8797612-8797891 | Common:1; Rare:112; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:9092048-9092103 | Rare:21 | ||||
| chr16:11976615-11976754 | Common:2; Rare:51 | ||||
| chr16:20806432-20806523 | Rare:38 | ||||
| chr16:23557291-23557465 | Common:2; Rare:73; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:23641249-23641543 | Common:2; Rare:86; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:25111446-25111767 | Common:2; Rare:75 | ||||
| chr16:27549892-27550165 | Common:2; Rare:100 | ||||
| chr16:28823979-28824122 | Common:1; Rare:38 | ||||
| chr16:28846281-28846729 | Common:2; Rare:142; Clinvar:5; Clinvar (benign):4 |