| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:88663070-88663374 | Common:8; Rare:125 | ||||
| chr16:88706204-88706512 | Common:3; Rare:134 | ||||
| chr16:88856882-88857153 | Common:4; Rare:127; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:89217619-89217754 | Common:1; Rare:63 | ||||
| chr16:89657637-89657846 | Common:1; Rare:104 | ||||
| chr16:89686665-89686701 | Common:3; Rare:22 | ||||
| chr16:89720865-89721004 | Common:1; Rare:40 | ||||
| chr16:89972462-89972645 | Common:1; Rare:66 | ||||
| chr16:90019355-90019691 | Common:6; Rare:101 | ||||
| chr17:714802-714882 | Common:1; Rare:29 | ||||
| chr17:752159-752302 | Common:2; Rare:61 | ||||
| chr17:1491602-1491816 | Common:1; Rare:63 | ||||
| chr17:1516588-1516978 | Common:2; Rare:137 | ||||
| chr17:1829828-1830042 | Common:7; Rare:89 | ||||
| chr17:2030012-2030181 | Common:1; Rare:65; Clinvar (pathogenic):1 |