| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:3577706-3577736 | Common:1; Rare:5 | ||||
| chr16:3611455-3611852 | Common:1; Rare:160; Clinvar:2 | ||||
| chr16:3717268-3717865 | Common:1; Rare:225; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:3880047-3880181 | Rare:38 | ||||
| chr16:3880613-3880952 | Common:4; Rare:106 | ||||
| chr16:4116382-4116702 | Common:2; Rare:117 | ||||
| chr16:4272339-4272400 | Rare:10 | ||||
| chr16:4272571-4272633 | Rare:23 | ||||
| chr16:4273284-4273539 | Common:1; Rare:66 | ||||
| chr16:4351227-4351538 | Common:2; Rare:136 | ||||
| chr16:4371573-4371903 | Common:1; Rare:111 | ||||
| chr16:4415858-4415954 | Rare:30 | ||||
| chr16:4416538-4416857 | Rare:98 | ||||
| chr16:4425388-4425556 | Rare:59 | ||||
| chr16:4425731-4425936 | Common:1; Rare:109 |