| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:142739428-142739554 | Common:1; Rare:33 | ||||
| chr8:143038928-143039294 | Common:3; Rare:139 | ||||
| chr8:143219663-143219941 | Common:5; Rare:36 | ||||
| chr8:143278732-143278837 | Common:1; Rare:46 | ||||
| chr8:143281563-143281835 | Common:7; Rare:115 | ||||
| chr8:143377105-143377450 | Common:3; Rare:102 | ||||
| chr8:143518950-143519280 | Common:9; Rare:110 | ||||
| chr8:143519290-143519570 | Rare:109 | ||||
| chr8:143739243-143739418 | Common:2; Rare:41 | ||||
| chr8:143739454-143739610 | Rare:72 | ||||
| chr8:143740535-143740763 | Common:2; Rare:96 | ||||
| chr8:143740683-143740985 | Common:2; Rare:80 | ||||
| chr8:143874251-143874679 | Common:8; Rare:198 | ||||
| chr8:143932601-143933320 | Common:8; Rare:385; Clinvar:48; Clinvar (benign):22 | ||||
| chr8:143943184-143943445 | Common:1; Rare:56 |