| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:56051371-56051899 | Common:1; Rare:191; Clinvar:5; Clinvar (benign):1 | ||||
| chr7:56064145-56064365 | Common:2; Rare:130 | ||||
| chr7:56106385-56106564 | Common:6; Rare:75 | ||||
| chr7:66114768-66114962 | Common:1; Rare:89 | ||||
| chr7:66115210-66115354 | Rare:31 | ||||
| chr7:66682028-66682175 | Common:5; Rare:71 | ||||
| chr7:66996557-66996888 | Common:2; Rare:77 | ||||
| chr7:73683399-73683628 | Common:3; Rare:96 | ||||
| chr7:73738786-73739036 | Common:1; Rare:75 | ||||
| chr7:73842491-73842699 | Common:6; Rare:34 | ||||
| chr7:74028050-74028170 | Common:1; Rare:39; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:74174043-74174393 | Common:1; Rare:163 | ||||
| chr7:74254366-74254528 | Rare:75 | ||||
| chr7:74453707-74454126 | Common:1; Rare:106 | ||||
| chr7:75878829-75879102 | Common:12; Rare:100 |