| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:149749567-149749785 | Rare:104 | ||||
| chr6:151452132-151452524 | Common:3; Rare:128 | ||||
| chr6:152983010-152983260 | Common:2; Rare:79 | ||||
| chr6:153002652-153002863 | Common:4; Rare:76 | ||||
| chr6:158168230-158168388 | Common:2; Rare:56 | ||||
| chr6:159726926-159727162 | Common:1; Rare:91 | ||||
| chr6:159789557-159789993 | Common:4; Rare:150 | ||||
| chr6:166342519-166342630 | Common:2; Rare:40 | ||||
| chr6:166999129-166999406 | Common:1; Rare:91 | ||||
| chr7:727252-727304 | Rare:14; Clinvar:1 | ||||
| chr7:1570007-1570080 | Common:1; Rare:24 | ||||
| chr7:2242171-2242245 | Common:2; Rare:46 | ||||
| chr7:23470357-23470557 | Rare:61 | ||||
| chr7:25125296-25125633 | Rare:124; Clinvar:2 | ||||
| chr7:30594756-30594909 | Common:1; Rare:70; Clinvar:4; Clinvar (benign):3 |