| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:68696445-68696653 | Common:4; Rare:40 | ||||
| chr16:68737266-68737454 | Common:1; Rare:72; Clinvar:8; Clinvar (benign):23 | ||||
| chr16:68808421-68808849 | Common:2; Rare:95; Clinvar:31; Clinvar (benign):22; Clinvar (pathogenic):1 | ||||
| chr16:69105342-69105687 | Rare:51 | ||||
| chr16:69106071-69106248 | Common:1; Rare:52 | ||||
| chr16:69132097-69132352 | Rare:49 | ||||
| chr16:69132494-69132697 | Rare:72 | ||||
| chr16:69311085-69311466 | Common:1; Rare:117 | ||||
| chr16:69330561-69330778 | Common:2; Rare:93 | ||||
| chr16:69339478-69339883 | Common:2; Rare:180; Clinvar:1; Clinvar (benign):4 | ||||
| chr16:69385396-69385620 | Common:1; Rare:73 | ||||
| chr16:69565858-69566032 | Common:2; Rare:66 | ||||
| chr16:69566315-69566352 | Rare:8 | ||||
| chr16:69726448-69726785 | Common:3; Rare:85 | ||||
| chr16:70251848-70252235 | Common:2; Rare:134 |