| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:152676083-152676295 | Common:2; Rare:92; Clinvar (benign):12 | ||||
| chr7:155644377-155644850 | Common:6; Rare:152 | ||||
| chr7:157336749-157337075 | Common:2; Rare:157; Clinvar:1 | ||||
| chr7:158704731-158705018 | Common:1; Rare:107 | ||||
| chr7:158856315-158856639 | Common:6; Rare:105 | ||||
| chr8:232181-232377 | Common:3; Rare:74 | ||||
| chr8:406828-406999 | Rare:69 | ||||
| chr8:731157-731436 | Common:3; Rare:109 | ||||
| chr8:2127584-2127800 | Common:7; Rare:37 | ||||
| chr8:6406518-6406670 | Common:3; Rare:83; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:6708155-6708350 | Common:2; Rare:74 | ||||
| chr8:6708505-6708693 | Common:1; Rare:78 | ||||
| chr8:8386390-8386562 | Common:3; Rare:72 | ||||
| chr8:9555651-9555942 | Common:6; Rare:110 | ||||
| chr8:10839799-10840095 | Common:3; Rare:101 |