| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:3053942-3053966 | Rare:4 | ||||
| chr16:3526426-3526556 | Common:3; Rare:33 | ||||
| chr16:4797959-4798184 | Rare:126; Clinvar:13; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:8862348-8862579 | Common:2; Rare:64 | ||||
| chr16:8894663-8894853 | Common:3; Rare:53 | ||||
| chr16:8954789-8954827 | Rare:11 | ||||
| chr16:9044469-9044515 | Rare:12 | ||||
| chr16:9068410-9068554 | Common:2; Rare:35 | ||||
| chr16:9094748-9095041 | Common:1; Rare:78 | ||||
| chr16:11839907-11840056 | Rare:57 | ||||
| chr16:14326358-14326437 | Rare:16 | ||||
| chr16:14449853-14450120 | Common:3; Rare:45 | ||||
| chr16:14486676-14486796 | Rare:13 | ||||
| chr16:15072851-15072988 | Common:1; Rare:30 | ||||
| chr16:16069095-16069363 | Common:12; Rare:68 |