| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:95024905-95025194 | Common:2; Rare:108; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr8:95133582-95133944 | Common:3; Rare:116 | ||||
| chr8:96235510-96235779 | Common:2; Rare:120; Clinvar (benign):2 | ||||
| chr8:96261566-96261967 | Common:6; Rare:135 | ||||
| chr8:96493509-96493823 | Rare:96 | ||||
| chr8:96494044-96494195 | Common:3; Rare:44 | ||||
| chr8:97644089-97644360 | Common:4; Rare:74 | ||||
| chr8:97775690-97776009 | Common:5; Rare:168; Clinvar (benign):1 | ||||
| chr8:98045333-98045679 | Common:4; Rare:103 | ||||
| chr8:98117103-98117379 | Common:4; Rare:90 | ||||
| chr8:99012977-99013102 | Rare:30 | ||||
| chr8:99013201-99013339 | Rare:28 | ||||
| chr8:100150555-100150709 | Rare:48 | ||||
| chr8:100309874-100310315 | Common:1; Rare:163 | ||||
| chr8:100950418-100950728 | Common:11; Rare:126 |