| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30699012-30699386 | Rare:98; Clinvar (benign):1 | ||||
| chr16:30748125-30748452 | Common:2; Rare:78; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:30762052-30762343 | Common:3; Rare:93 | ||||
| chr16:30787119-30787211 | Rare:15 | ||||
| chr16:30893923-30894268 | Common:5; Rare:93 | ||||
| chr16:30896438-30896646 | Common:1; Rare:51 | ||||
| chr16:30923145-30923151 | Rare:1 | ||||
| chr16:30923236-30923592 | Common:1; Rare:87 | ||||
| chr16:30949057-30949118 | Rare:12 | ||||
| chr16:30957636-30957765 | Common:1; Rare:40 | ||||
| chr16:30997280-30997411 | Common:1; Rare:31 | ||||
| chr16:31032877-31033099 | Common:1; Rare:46 | ||||
| chr16:31033373-31033783 | Common:1; Rare:123 | ||||
| chr16:31073690-31073848 | Rare:51 | ||||
| chr16:31074187-31074462 | Common:1; Rare:76 |