| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:152759642-152759863 | Common:4; Rare:92 | ||||
| chr7:154304972-154305196 | Common:4; Rare:71 | ||||
| chr7:155644336-155644897 | Common:6; Rare:178 | ||||
| chr7:156640529-156640791 | Common:3; Rare:127 | ||||
| chr7:157336770-157337149 | Common:3; Rare:176; Clinvar:3; Clinvar (benign):2 | ||||
| chr7:158704740-158704986 | Common:1; Rare:86 | ||||
| chr7:158856423-158856687 | Common:7; Rare:94 | ||||
| chr8:232152-232482 | Common:3; Rare:138 | ||||
| chr8:233037-233189 | Common:1; Rare:34 | ||||
| chr8:406834-407027 | Rare:78 | ||||
| chr8:731159-731416 | Common:3; Rare:96 | ||||
| chr8:1973857-1973922 | Rare:26 | ||||
| chr8:2127569-2127822 | Common:9; Rare:54 | ||||
| chr8:4994580-4994818 | Rare:74 | ||||
| chr8:6406465-6406688 | Common:5; Rare:118; Clinvar:2; Clinvar (benign):1 |