| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144291348-144291668 | Common:1; Rare:104 | ||||
| chr8:144409233-144409556 | Common:1; Rare:106 | ||||
| chr8:144427266-144427460 | Rare:56 | ||||
| chr8:144428444-144428648 | Common:2; Rare:81 | ||||
| chr8:144444397-144444584 | Rare:59 | ||||
| chr8:144465320-144465503 | Common:4; Rare:68 | ||||
| chr8:144477871-144478102 | Common:5; Rare:85 | ||||
| chr8:144508922-144509122 | Rare:61 | ||||
| chr8:144517724-144518023 | Common:1; Rare:110; Clinvar:10; Clinvar (benign):1 | ||||
| chr8:144755443-144755729 | Common:1; Rare:100 | ||||
| chr8:144787270-144787392 | Rare:39 | ||||
| chr8:144792335-144792590 | Common:3; Rare:102 | ||||
| chr8:144798802-144798924 | Common:1; Rare:34 | ||||
| chr8:144827235-144827608 | Common:2; Rare:96 | ||||
| chr8:144901365-144901636 | Common:1; Rare:82 |