| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31330139-31330574 | Rare:141 | ||||
| chr16:31355042-31355257 | Common:1; Rare:63 | ||||
| chr16:31442772-31443059 | Common:1; Rare:47 | ||||
| chr16:31458897-31459517 | Common:2; Rare:211 | ||||
| chr16:31472109-31472191 | Rare:23 | ||||
| chr16:31508374-31508484 | Common:2; Rare:43 | ||||
| chr16:46689116-46689317 | Common:1; Rare:75; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46973496-46973810 | Rare:122 | ||||
| chr16:47460987-47461378 | Common:2; Rare:161; Clinvar (benign):2 | ||||
| chr16:48244257-48244379 | Common:1; Rare:44 | ||||
| chr16:48244381-48244598 | Rare:55 | ||||
| chr16:48347982-48348200 | Rare:48 | ||||
| chr16:48385302-48385561 | Common:3; Rare:106 | ||||
| chr16:48609911-48610285 | Common:2; Rare:129 | ||||
| chr16:50065832-50066032 | Common:4; Rare:69 |