| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30698461-30698723 | Common:1; Rare:96 | ||||
| chr16:30698969-30699402 | Rare:122; Clinvar (benign):1 | ||||
| chr16:30748108-30748457 | Common:2; Rare:83; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:30761454-30761612 | Rare:63 | ||||
| chr16:30762052-30762352 | Common:3; Rare:96 | ||||
| chr16:30893898-30894339 | Common:5; Rare:114 | ||||
| chr16:30922558-30922904 | Common:1; Rare:93 | ||||
| chr16:30923238-30923598 | Common:1; Rare:87 | ||||
| chr16:30957567-30957787 | Common:1; Rare:64 | ||||
| chr16:31033298-31033606 | Common:2; Rare:101 | ||||
| chr16:31073693-31073838 | Rare:48 | ||||
| chr16:31074183-31074483 | Common:2; Rare:84 | ||||
| chr16:31094560-31095050 | Common:1; Rare:150; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr16:31108282-31108471 | Rare:42 | ||||
| chr16:31180600-31180847 | Common:3; Rare:92 |