| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30985048-30985273 | Rare:63 | ||||
| chr16:31032854-31033095 | Common:1; Rare:48 | ||||
| chr16:31033432-31033810 | Common:1; Rare:114 | ||||
| chr16:31073726-31073800 | Rare:22 | ||||
| chr16:31074177-31074502 | Common:2; Rare:88 | ||||
| chr16:31117892-31118059 | Rare:41 | ||||
| chr16:31135419-31135589 | Common:1; Rare:40 | ||||
| chr16:31202641-31202706 | Rare:20 | ||||
| chr16:31442753-31443059 | Common:1; Rare:51 | ||||
| chr16:31458887-31459161 | Rare:78 | ||||
| chr16:31459290-31459517 | Common:1; Rare:94 | ||||
| chr16:31471931-31472200 | Rare:63 | ||||
| chr16:31507864-31508031 | Common:1; Rare:62 | ||||
| chr16:31508323-31508516 | Common:4; Rare:89 | ||||
| chr16:46689130-46689317 | Common:1; Rare:72; Clinvar:2; Clinvar (benign):1 |