| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30585687-30585885 | Common:1; Rare:37 | ||||
| chr16:30698466-30698590 | Common:1; Rare:53 | ||||
| chr16:30748109-30748441 | Common:2; Rare:78; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:30762060-30762335 | Common:3; Rare:93 | ||||
| chr16:30787146-30787271 | Rare:17 | ||||
| chr16:30923256-30923612 | Common:1; Rare:83 | ||||
| chr16:31033486-31033569 | Rare:32 | ||||
| chr16:31074187-31074442 | Common:1; Rare:71 | ||||
| chr16:31094703-31094797 | Rare:36 | ||||
| chr16:31108268-31108465 | Rare:42 | ||||
| chr16:31442766-31443059 | Common:1; Rare:47 | ||||
| chr16:31459310-31459517 | Common:1; Rare:85 | ||||
| chr16:31472109-31472189 | Rare:22 | ||||
| chr16:31508374-31508484 | Common:2; Rare:43 | ||||
| chr16:46689129-46689416 | Common:1; Rare:102; Clinvar:2; Clinvar (benign):1 |