| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:46689129-46689416 | Common:1; Rare:102; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46689504-46689708 | Common:2; Rare:83; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:46789926-46790093 | Common:4; Rare:40 | ||||
| chr16:46973577-46973802 | Rare:101 | ||||
| chr16:47460836-47461398 | Common:3; Rare:221; Clinvar (benign):3 | ||||
| chr16:48244253-48244621 | Common:2; Rare:107 | ||||
| chr16:49281731-49282068 | Common:2; Rare:102 | ||||
| chr16:50024887-50025324 | Common:5; Rare:128 | ||||
| chr16:50741661-50741914 | Common:4; Rare:69 | ||||
| chr16:53098901-53099189 | Rare:64 | ||||
| chr16:53208305-53208512 | Rare:43 | ||||
| chr16:53434393-53434692 | Common:1; Rare:124 | ||||
| chr16:53703809-53704227 | Common:1; Rare:133; Clinvar:4; Clinvar (benign):2 | ||||
| chr16:54286718-54287016 | Common:1; Rare:88 | ||||
| chr16:56191596-56191952 | Common:1; Rare:87 |