| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:93700426-93700627 | Common:1; Rare:81 | ||||
| chr8:93916628-93917001 | Common:4; Rare:132; Clinvar:1; Clinvar (benign):1 | ||||
| chr8:94553443-94553737 | Common:3; Rare:104 | ||||
| chr8:94640728-94641450 | Common:7; Rare:211 | ||||
| chr8:94719780-94719955 | Common:1; Rare:50 | ||||
| chr8:94895194-94895331 | Rare:46 | ||||
| chr8:94895688-94895816 | Common:1; Rare:36 | ||||
| chr8:94949329-94949520 | Common:1; Rare:58 | ||||
| chr8:95024905-95025109 | Common:2; Rare:88; Clinvar:1; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr8:95268609-95268837 | Common:8; Rare:56 | ||||
| chr8:95269190-95269449 | Common:10; Rare:85; Clinvar:1 | ||||
| chr8:96235514-96235643 | Common:1; Rare:68; Clinvar (benign):2 | ||||
| chr8:96261553-96261979 | Common:6; Rare:144 | ||||
| chr8:97644089-97644315 | Common:4; Rare:60 | ||||
| chr8:97775720-97775995 | Common:4; Rare:141; Clinvar (benign):1 |