| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:4371693-4371851 | Rare:57 | ||||
| chr16:4425737-4425929 | Common:1; Rare:102 | ||||
| chr16:4476266-4476466 | Common:3; Rare:74 | ||||
| chr16:4538390-4538634 | Common:4; Rare:83 | ||||
| chr16:4538752-4538919 | Rare:66 | ||||
| chr16:4614871-4615085 | Common:1; Rare:65 | ||||
| chr16:4616115-4616632 | Common:1; Rare:144 | ||||
| chr16:4624573-4624886 | Common:1; Rare:116 | ||||
| chr16:4693476-4693721 | Common:2; Rare:103 | ||||
| chr16:4734151-4734298 | Common:1; Rare:50 | ||||
| chr16:4767120-4767330 | Common:2; Rare:70 | ||||
| chr16:5033922-5033976 | Rare:21 | ||||
| chr16:5071778-5071911 | Rare:80; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr16:5097737-5097977 | Common:4; Rare:91 | ||||
| chr16:6019452-6019713 | Common:1; Rare:93 |