| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:19555455-19555729 | Common:1; Rare:123 | ||||
| chr16:19862017-19862320 | Rare:51 | ||||
| chr16:20806331-20806659 | Rare:103 | ||||
| chr16:20900226-20900873 | Common:4; Rare:154 | ||||
| chr16:21652602-21652622 | Rare:10 | ||||
| chr16:21952991-21953419 | Common:1; Rare:109; Clinvar (benign):3 | ||||
| chr16:22297230-22297460 | Common:2; Rare:95 | ||||
| chr16:22436942-22437061 | Rare:43 | ||||
| chr16:22437103-22437313 | Rare:69 | ||||
| chr16:23182690-23182756 | Rare:15 | ||||
| chr16:23453127-23453240 | Rare:31 | ||||
| chr16:23557333-23557452 | Rare:45; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:23641247-23641525 | Common:2; Rare:80; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:23678714-23678935 | Common:4; Rare:68 | ||||
| chr16:24255778-24256076 | Common:1; Rare:68 |