| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:3400991-3401226 | Common:5; Rare:86 | ||||
| chr16:3443452-3443725 | Common:3; Rare:89 | ||||
| chr16:3457946-3458111 | Common:2; Rare:79 | ||||
| chr16:4425767-4425888 | Common:1; Rare:56 | ||||
| chr16:4476273-4476459 | Common:3; Rare:68 | ||||
| chr16:4693478-4693735 | Common:2; Rare:114 | ||||
| chr16:4734204-4734534 | Rare:108 | ||||
| chr16:4767134-4767330 | Common:1; Rare:65 | ||||
| chr16:5071783-5071849 | Rare:30; Clinvar (benign):1 | ||||
| chr16:8797631-8797895 | Rare:103; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:8868971-8869261 | Common:4; Rare:128 | ||||
| chr16:10944333-10944582 | Common:1; Rare:73 | ||||
| chr16:11586893-11587018 | Common:1; Rare:39 | ||||
| chr16:11851499-11851645 | Rare:71 | ||||
| chr16:11976615-11976760 | Common:2; Rare:53 |