| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144500988-144501290 | Rare:150 | ||||
| chr8:144503287-144503467 | Common:1; Rare:44 | ||||
| chr8:144503985-144504163 | Rare:39 | ||||
| chr8:144517700-144518014 | Common:1; Rare:107; Clinvar:10; Clinvar (benign):2 | ||||
| chr8:144755429-144755647 | Common:1; Rare:82 | ||||
| chr8:144792304-144792585 | Common:3; Rare:109 | ||||
| chr8:144798809-144798922 | Common:1; Rare:32 | ||||
| chr8:144853008-144853352 | Common:2; Rare:102 | ||||
| chr8:144901406-144901755 | Common:1; Rare:98 | ||||
| chr8:144902093-144902141 | Rare:11 | ||||
| chr8:144950590-144950672 | Common:1; Rare:22 | ||||
| chr8:145052106-145052500 | Common:11; Rare:99 | ||||
| chr9:214697-214868 | Common:4; Rare:95; Clinvar (benign):1 | ||||
| chr9:470139-470350 | Common:16; Rare:90 | ||||
| chr9:2015071-2015398 | Common:3; Rare:95 |