| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30698979-30699191 | Rare:78; Clinvar (benign):1 | ||||
| chr16:30761433-30761563 | Rare:45 | ||||
| chr16:30762060-30762334 | Common:3; Rare:93 | ||||
| chr16:30787146-30787286 | Rare:20 | ||||
| chr16:30893911-30894268 | Common:5; Rare:95 | ||||
| chr16:30923242-30923608 | Common:1; Rare:88 | ||||
| chr16:31033460-31033617 | Common:1; Rare:57 | ||||
| chr16:31039077-31039344 | Rare:37 | ||||
| chr16:31074167-31074450 | Common:2; Rare:82 | ||||
| chr16:31458897-31459161 | Rare:76 | ||||
| chr16:31471931-31472191 | Rare:60 | ||||
| chr16:31508365-31508490 | Common:4; Rare:52 | ||||
| chr16:46689101-46689304 | Common:1; Rare:83; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46689489-46689722 | Common:2; Rare:96; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:46973568-46973753 | Rare:79 |