| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:151240213-151240437 | Common:2; Rare:58 | ||||
| chr6:151240840-151241015 | Common:2; Rare:52 | ||||
| chr6:151391815-151391956 | Rare:48 | ||||
| chr6:151451991-151452550 | Common:5; Rare:194; Clinvar (benign):3 | ||||
| chr6:151493982-151494132 | Common:1; Rare:50 | ||||
| chr6:152302096-152302236 | Rare:43 | ||||
| chr6:152381273-152381406 | Rare:43; Clinvar:5; Clinvar (pathogenic):1 | ||||
| chr6:152983018-152983353 | Common:2; Rare:104 | ||||
| chr6:152983494-152983808 | Common:4; Rare:119 | ||||
| chr6:153002666-153002870 | Common:4; Rare:68 | ||||
| chr6:153131192-153131519 | Rare:140 | ||||
| chr6:154510561-154510908 | Common:3; Rare:108 | ||||
| chr6:154733164-154733428 | Rare:109 | ||||
| chr6:154734168-154734325 | Common:5; Rare:43 | ||||
| chr6:154995020-154995430 | Common:5; Rare:108 |