| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:88710028-88710244 | Common:1; Rare:93 | ||||
| chr16:88716265-88716571 | Common:2; Rare:146; Clinvar (benign):2 | ||||
| chr16:88717229-88717386 | Common:1; Rare:58 | ||||
| chr16:88717937-88718231 | Common:4; Rare:115 | ||||
| chr16:88785179-88785309 | Common:1; Rare:50 | ||||
| chr16:88811885-88811981 | Common:2; Rare:57; Clinvar (benign):1 | ||||
| chr16:88856867-88857188 | Common:4; Rare:158; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:89217599-89217752 | Common:1; Rare:75 | ||||
| chr16:89490537-89490695 | Common:2; Rare:66 | ||||
| chr16:89508262-89508445 | Common:2; Rare:106; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:89560541-89560782 | Rare:106 | ||||
| chr16:89562366-89562527 | Common:3; Rare:58 | ||||
| chr16:89584852-89584889 | Rare:20 | ||||
| chr16:89657617-89658111 | Common:4; Rare:255; Clinvar (benign):1 | ||||
| chr16:89686898-89686955 | Rare:24 |