| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30698466-30698639 | Common:1; Rare:67 | ||||
| chr16:30699035-30699362 | Rare:81; Clinvar (benign):1 | ||||
| chr16:30748128-30748441 | Common:2; Rare:74; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:30762060-30762348 | Common:3; Rare:94 | ||||
| chr16:30787165-30787302 | Rare:23 | ||||
| chr16:30893960-30894275 | Common:5; Rare:84 | ||||
| chr16:31073740-31073800 | Rare:14 | ||||
| chr16:31074187-31074436 | Common:1; Rare:68 | ||||
| chr16:31108288-31108465 | Rare:41 | ||||
| chr16:31459319-31459469 | Common:1; Rare:64 | ||||
| chr16:31508374-31508508 | Common:4; Rare:55 | ||||
| chr16:46621325-46621480 | Rare:55 | ||||
| chr16:46689134-46689384 | Common:1; Rare:90; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46973581-46973796 | Rare:98 | ||||
| chr16:47461046-47461365 | Common:2; Rare:115; Clinvar (benign):2 |