| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31458504-31458884 | Common:4; Rare:107 | ||||
| chr16:31458982-31459568 | Common:3; Rare:207 | ||||
| chr16:31459648-31460111 | Common:1; Rare:216 | ||||
| chr16:31508320-31508701 | Common:5; Rare:129 | ||||
| chr16:31713051-31713405 | Common:1; Rare:83 | ||||
| chr16:31713509-31713648 | Common:2; Rare:46 | ||||
| chr16:31873589-31873907 | Common:1; Rare:100 | ||||
| chr16:31874074-31874203 | Rare:27 | ||||
| chr16:46621274-46621530 | Common:1; Rare:100 | ||||
| chr16:46688622-46688790 | Rare:41 | ||||
| chr16:46689092-46689333 | Common:1; Rare:96; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46689436-46689744 | Common:3; Rare:115; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:46689842-46689940 | Rare:26 | ||||
| chr16:46690110-46690261 | Rare:36 | ||||
| chr16:46789875-46790199 | Common:5; Rare:78 |