| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30697933-30698231 | Common:1; Rare:134 | ||||
| chr16:30698455-30698598 | Common:1; Rare:60 | ||||
| chr16:30709721-30709885 | Rare:35 | ||||
| chr16:30748125-30748462 | Common:2; Rare:82; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:30762060-30762348 | Common:3; Rare:94 | ||||
| chr16:30893951-30894281 | Common:5; Rare:89 | ||||
| chr16:30923236-30923585 | Common:1; Rare:85 | ||||
| chr16:30949123-30949295 | Common:3; Rare:49 | ||||
| chr16:30997284-30997447 | Common:1; Rare:38 | ||||
| chr16:31033460-31033606 | Common:1; Rare:55 | ||||
| chr16:31073703-31073848 | Rare:47 | ||||
| chr16:31074182-31074450 | Common:2; Rare:73 | ||||
| chr16:31117911-31118059 | Rare:38 | ||||
| chr16:31202686-31202918 | Common:2; Rare:85 | ||||
| chr16:31442772-31443059 | Common:1; Rare:47 |