| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:72811710-72811925 | Common:2; Rare:67 | ||||
| chr16:74368127-74368376 | Common:1; Rare:69 | ||||
| chr16:79505265-79505593 | Common:4; Rare:77 | ||||
| chr16:79598010-79598335 | Common:4; Rare:79 | ||||
| chr16:79598529-79598796 | Common:9; Rare:78 | ||||
| chr16:79598937-79598957 | Rare:6 | ||||
| chr16:79770551-79770726 | Common:5; Rare:79 | ||||
| chr16:87956355-87956532 | Common:1; Rare:49 | ||||
| chr16:88186716-88186830 | Common:1; Rare:35 | ||||
| chr16:88721589-88721854 | Common:5; Rare:140 | ||||
| chr16:89362709-89363012 | Common:7; Rare:63 | ||||
| chr16:90102175-90102304 | Common:4; Rare:40 | ||||
| chr17:1774882-1775198 | Common:2; Rare:116; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr17:3665081-3665180 | Common:1; Rare:12 | ||||
| chr17:3921690-3921868 | Rare:51 |