| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:3500851-3501096 | Common:8; Rare:170 | ||||
| chr16:3611454-3611884 | Common:2; Rare:418; Clinvar:6 | ||||
| chr16:3642779-3643001 | Rare:115 | ||||
| chr16:3655023-3656051 | Common:11; Rare:663 | ||||
| chr16:3716681-3717081 | Common:1; Rare:135 | ||||
| chr16:3717418-3717939 | Common:3; Rare:416; Clinvar:3; Clinvar (benign):3 | ||||
| chr16:3879570-3880230 | Common:2; Rare:342 | ||||
| chr16:3880514-3880998 | Common:10; Rare:310 | ||||
| chr16:4115720-4115984 | Common:3; Rare:176 | ||||
| chr16:4116220-4116775 | Common:8; Rare:435 | ||||
| chr16:4272791-4273420 | Common:3; Rare:199 | ||||
| chr16:4315257-4315778 | Common:3; Rare:144 | ||||
| chr16:4350500-4351020 | Common:2; Rare:140 | ||||
| chr16:4351177-4351549 | Common:4; Rare:299 | ||||
| chr16:4371690-4371867 | Rare:123 |