| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:17922677-17923009 | Common:4; Rare:131 | ||||
| chr8:18084820-18085028 | Common:2; Rare:58; Clinvar (benign):1 | ||||
| chr8:18684039-18684157 | Rare:29 | ||||
| chr8:18854300-18854388 | Rare:18 | ||||
| chr8:18887023-18887126 | Rare:15 | ||||
| chr8:19602205-19602319 | Common:2; Rare:34 | ||||
| chr8:20197118-20197537 | Common:2; Rare:188 | ||||
| chr8:22245024-22245157 | Rare:70 | ||||
| chr8:22367188-22367331 | Common:5; Rare:65 | ||||
| chr8:22589152-22589348 | Common:1; Rare:74 | ||||
| chr8:22604584-22604820 | Common:1; Rare:94 | ||||
| chr8:22669082-22669207 | Common:2; Rare:41 | ||||
| chr8:23457601-23457778 | Common:3; Rare:68 | ||||
| chr8:23528724-23529075 | Rare:108 | ||||
| chr8:24294023-24294131 | Rare:23 |