| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:78264025-78264130 | Rare:17 | ||||
| chr16:78508344-78508549 | Common:2; Rare:62 | ||||
| chr16:79597894-79598571 | Common:8; Rare:150 | ||||
| chr16:79598952-79599206 | Common:2; Rare:75; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr16:79645401-79645577 | Common:1; Rare:43 | ||||
| chr16:80982219-80982511 | Common:3; Rare:82 | ||||
| chr16:81382394-81382554 | Common:2; Rare:38 | ||||
| chr16:81383426-81383552 | Common:1; Rare:30 | ||||
| chr16:81384309-81384568 | Common:3; Rare:66 | ||||
| chr16:81401085-81401258 | Common:1; Rare:47 | ||||
| chr16:81452531-81452579 | Common:1; Rare:13 | ||||
| chr16:81470465-81470553 | Rare:19 | ||||
| chr16:81503736-81503989 | Common:1; Rare:54 | ||||
| chr16:81526853-81526945 | Rare:16 | ||||
| chr16:81539098-81539271 | Rare:50 |