| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:134713017-134713115 | Common:1; Rare:29 | ||||
| chr8:143018380-143018579 | Common:2; Rare:59 | ||||
| chr8:143541430-143541643 | Common:2; Rare:69 | ||||
| chr8:143558262-143558383 | Common:1; Rare:43 | ||||
| chr8:143635969-143636058 | Common:1; Rare:37 | ||||
| chr8:144078474-144078734 | Common:1; Rare:81 | ||||
| chr8:144082524-144082670 | Common:2; Rare:51 | ||||
| chr8:144103692-144103872 | Common:1; Rare:64 | ||||
| chr8:144428497-144428638 | Common:2; Rare:51 | ||||
| chr8:144755429-144755637 | Common:1; Rare:80 | ||||
| chr8:144787305-144787414 | Rare:35 | ||||
| chr8:144950817-144950912 | Common:1; Rare:33 | ||||
| chr8:145052114-145052434 | Common:11; Rare:62 | ||||
| chr9:707004-707161 | Common:3; Rare:49 | ||||
| chr9:2621848-2622183 | Common:6; Rare:120; Clinvar:9; Clinvar (benign):3 |