| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:5071773-5071843 | Rare:31; Clinvar (benign):1 | ||||
| chr16:8797631-8797866 | Rare:88; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:8868982-8869269 | Common:4; Rare:128 | ||||
| chr16:10580627-10580841 | Common:2; Rare:76 | ||||
| chr16:10743726-10743869 | Rare:58 | ||||
| chr16:10944327-10944591 | Common:1; Rare:77 | ||||
| chr16:11586908-11587017 | Common:1; Rare:35 | ||||
| chr16:11851507-11851653 | Rare:70 | ||||
| chr16:11915900-11916212 | Common:2; Rare:126 | ||||
| chr16:11976615-11976760 | Common:2; Rare:53 | ||||
| chr16:14630188-14630377 | Rare:88 | ||||
| chr16:14632649-14632983 | Common:1; Rare:113 | ||||
| chr16:15094247-15094429 | Rare:82 | ||||
| chr16:15888572-15888724 | Common:2; Rare:68 | ||||
| chr16:18801456-18801830 | Common:4; Rare:132 |