| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:75647541-75647894 | Common:12; Rare:426; Clinvar:12; Clinvar (pathogenic):2 | ||||
| chr16:75648546-75648701 | Rare:70 | ||||
| chr16:75648610-75648757 | Rare:98 | ||||
| chr16:77190414-77190730 | Common:5; Rare:86 | ||||
| chr16:77190667-77191308 | Common:33; Rare:499 | ||||
| chr16:77211826-77212816 | Common:16; Rare:429 | ||||
| chr16:77722243-77722692 | Common:13; Rare:351 | ||||
| chr16:78099236-78099905 | Common:12; Rare:762; Clinvar:7; Clinvar (benign):22 | ||||
| chr16:79599813-79600300 | Common:10; Rare:238; Clinvar (benign):1 | ||||
| chr16:79600670-79600972 | Common:4; Rare:205 | ||||
| chr16:80540410-80540720 | Rare:201 | ||||
| chr16:80540740-80541120 | Common:15; Rare:446 | ||||
| chr16:80803630-80804040 | Common:2; Rare:93 | ||||
| chr16:80804060-80804450 | Common:1; Rare:177 | ||||
| chr16:80804399-80804738 | Common:7; Rare:257 |