| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:37762509-37762672 | Common:2; Rare:65 | ||||
| chr8:38030260-38030589 | Common:3; Rare:94 | ||||
| chr8:38105435-38105556 | Common:1; Rare:42 | ||||
| chr8:38176430-38176535 | Common:1; Rare:39 | ||||
| chr8:38176681-38176881 | Common:2; Rare:58 | ||||
| chr8:38269125-38269283 | Rare:61 | ||||
| chr8:38728536-38728602 | Rare:12 | ||||
| chr8:38901691-38901822 | Common:3; Rare:22 | ||||
| chr8:38996443-38997066 | Common:7; Rare:236 | ||||
| chr8:40153226-40153482 | Common:1; Rare:48 | ||||
| chr8:42391697-42391925 | Common:3; Rare:81 | ||||
| chr8:42541131-42541179 | Rare:10 | ||||
| chr8:42541494-42541658 | Common:2; Rare:44 | ||||
| chr8:42541691-42542037 | Common:1; Rare:106; Clinvar:3; Clinvar (benign):1 | ||||
| chr8:42843289-42843502 | Common:2; Rare:59; Clinvar (benign):3 |