| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30748118-30748441 | Common:2; Rare:76; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:30761454-30761604 | Rare:61 | ||||
| chr16:30762151-30762327 | Common:3; Rare:73 | ||||
| chr16:30923251-30923585 | Common:1; Rare:82 | ||||
| chr16:31033450-31033576 | Rare:49 | ||||
| chr16:31074187-31074451 | Common:1; Rare:73 | ||||
| chr16:31094699-31094768 | Rare:27 | ||||
| chr16:31094770-31094997 | Rare:58; Clinvar:1 | ||||
| chr16:31108282-31108465 | Rare:41 | ||||
| chr16:31179820-31180174 | Common:2; Rare:144; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:31180596-31180871 | Common:3; Rare:101 | ||||
| chr16:31202288-31202390 | Common:2; Rare:28 | ||||
| chr16:31202716-31203049 | Common:2; Rare:104 | ||||
| chr16:31459091-31459150 | Rare:20 | ||||
| chr16:31459288-31459510 | Common:1; Rare:93 |