| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144755432-144755680 | Common:1; Rare:90 | ||||
| chr8:144787288-144787374 | Rare:27 | ||||
| chr8:144792335-144792562 | Common:3; Rare:85 | ||||
| chr8:144852970-144853156 | Rare:66 | ||||
| chr8:144853482-144853707 | Common:2; Rare:53 | ||||
| chr8:144901390-144901613 | Common:1; Rare:68 | ||||
| chr8:144950817-144950912 | Common:1; Rare:33 | ||||
| chr8:145052193-145052530 | Common:10; Rare:105 | ||||
| chr9:178938-179107 | Common:5; Rare:38 | ||||
| chr9:470136-470371 | Common:16; Rare:102 | ||||
| chr9:2015048-2015396 | Common:3; Rare:102 | ||||
| chr9:2017376-2017449 | Rare:19 | ||||
| chr9:2158140-2158511 | Common:1; Rare:77 | ||||
| chr9:2160378-2160648 | Rare:84 | ||||
| chr9:2181363-2181575 | Common:2; Rare:71; Clinvar (benign):1 |