| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:69132547-69132671 | Rare:52 | ||||
| chr16:69311097-69311428 | Rare:99 | ||||
| chr16:69339568-69339821 | Common:1; Rare:99; Clinvar (benign):1 | ||||
| chr16:69424478-69424678 | Rare:57 | ||||
| chr16:69726431-69726780 | Common:4; Rare:93 | ||||
| chr16:69754885-69755116 | Rare:84 | ||||
| chr16:69762250-69762381 | Common:1; Rare:36 | ||||
| chr16:70114127-70114368 | Common:3; Rare:88 | ||||
| chr16:70289446-70289760 | Common:2; Rare:130; Clinvar:1 | ||||
| chr16:70299093-70299259 | Common:1; Rare:36 | ||||
| chr16:70346759-70346947 | Common:1; Rare:91 | ||||
| chr16:70454521-70454619 | Common:1; Rare:29 | ||||
| chr16:70523527-70523837 | Common:3; Rare:100; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr16:71564926-71565016 | Rare:31 | ||||
| chr16:71808774-71808875 | Common:1; Rare:58 |