| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:75556069-75556360 | Common:3; Rare:105; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr16:75566179-75566439 | Common:2; Rare:117 | ||||
| chr16:75623208-75623390 | Common:4; Rare:70 | ||||
| chr16:75647605-75647837 | Common:2; Rare:114; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:75648096-75648257 | Rare:68 | ||||
| chr16:77190702-77191042 | Common:10; Rare:108 | ||||
| chr16:77191133-77191269 | Common:1; Rare:53 | ||||
| chr16:77722281-77722556 | Common:4; Rare:86 | ||||
| chr16:78099394-78099823 | Common:2; Rare:184; Clinvar (benign):7 | ||||
| chr16:79599793-79599898 | Rare:19 | ||||
| chr16:79599942-79600160 | Common:3; Rare:63 | ||||
| chr16:79600689-79600968 | Common:1; Rare:78 | ||||
| chr16:79601029-79601239 | Common:2; Rare:60 | ||||
| chr16:80540908-80541057 | Common:3; Rare:61 | ||||
| chr16:81006429-81006598 | Rare:56 |