| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:130206467-130206584 | Common:1; Rare:21 | ||||
| chr8:130264391-130264471 | Rare:15 | ||||
| chr8:130313302-130313615 | Common:2; Rare:50 | ||||
| chr8:130428598-130428873 | Common:2; Rare:59 | ||||
| chr8:140633902-140634263 | Common:1; Rare:60 | ||||
| chr8:141000038-141000119 | Rare:5 | ||||
| chr8:143281596-143281904 | Common:3; Rare:72 | ||||
| chr8:143579789-143580034 | Rare:78; Clinvar:1 | ||||
| chr8:144360381-144360645 | Rare:92; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):5 | ||||
| chr8:144685802-144686043 | Common:3; Rare:58 | ||||
| chr8:144789905-144790010 | Rare:25 | ||||
| chr8:144826768-144826873 | Common:1; Rare:26 | ||||
| chr8:145002827-145003067 | Common:2; Rare:85 | ||||
| chr9:693593-693714 | Rare:34 | ||||
| chr9:3524425-3524712 | Common:1; Rare:80 |