| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:3611558-3611828 | Common:1; Rare:112; Clinvar:1 | ||||
| chr16:3717480-3717630 | Rare:75; Clinvar:1 | ||||
| chr16:4351253-4351533 | Common:2; Rare:121 | ||||
| chr16:4371693-4371872 | Rare:67 | ||||
| chr16:4425734-4425923 | Common:1; Rare:101 | ||||
| chr16:4476273-4476483 | Common:3; Rare:79 | ||||
| chr16:4538389-4538644 | Common:4; Rare:86 | ||||
| chr16:4538741-4538919 | Rare:69 | ||||
| chr16:4614866-4615003 | Common:1; Rare:36 | ||||
| chr16:4624580-4624874 | Common:1; Rare:110 | ||||
| chr16:4693482-4693729 | Common:2; Rare:108 | ||||
| chr16:4734125-4734545 | Common:1; Rare:139 | ||||
| chr16:4767120-4767384 | Common:2; Rare:88 | ||||
| chr16:4802815-4803083 | Common:2; Rare:128; Clinvar:3; Clinvar (benign):1 | ||||
| chr16:5033928-5033992 | Rare:23 |