| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:88570166-88570482 | Common:2; Rare:120 | ||||
| chr16:88663078-88663374 | Common:8; Rare:121 | ||||
| chr16:88706192-88706510 | Common:3; Rare:138 | ||||
| chr16:88856937-88857148 | Common:4; Rare:92; Clinvar (benign):2 | ||||
| chr16:89217627-89217749 | Common:1; Rare:54 | ||||
| chr16:89508318-89508424 | Rare:59; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr16:89560564-89560716 | Rare:62 | ||||
| chr16:89657638-89658086 | Common:3; Rare:236 | ||||
| chr16:89686567-89686704 | Common:6; Rare:61 | ||||
| chr16:89720865-89720985 | Common:1; Rare:32 | ||||
| chr16:89816647-89816758 | Common:2; Rare:44; Clinvar:1 | ||||
| chr16:89873469-89873789 | Common:2; Rare:148 | ||||
| chr16:89972478-89972658 | Common:1; Rare:66 | ||||
| chr16:90022552-90022711 | Rare:63 | ||||
| chr17:352772-352836 | Common:1; Rare:15 |