| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30661197-30661245 | Rare:17 | ||||
| chr16:30697974-30698282 | Common:1; Rare:141 | ||||
| chr16:30698408-30698534 | Rare:59 | ||||
| chr16:30698565-30698739 | Common:1; Rare:53 | ||||
| chr16:30698889-30699374 | Rare:150; Clinvar (benign):1 | ||||
| chr16:30699405-30699560 | Common:1; Rare:41 | ||||
| chr16:30740388-30740658 | Rare:50 | ||||
| chr16:30748049-30748326 | Common:1; Rare:69 | ||||
| chr16:30748356-30748500 | Common:1; Rare:45; Clinvar:2; Clinvar (benign):3 | ||||
| chr16:30748741-30748848 | Rare:33; Clinvar:1 | ||||
| chr16:30762027-30762363 | Common:3; Rare:108 | ||||
| chr16:30786747-30786970 | Common:2; Rare:50 | ||||
| chr16:30787129-30787389 | Common:1; Rare:47 | ||||
| chr16:30787481-30787518 | Rare:4 | ||||
| chr16:30893972-30894420 | Common:5; Rare:116 |