| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:37744321-37744632 | Common:1; Rare:78; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr8:37747976-37748111 | Rare:52 | ||||
| chr8:38091394-38091563 | Common:2; Rare:28 | ||||
| chr8:38382959-38383074 | Common:1; Rare:28 | ||||
| chr8:38560941-38561053 | Common:2; Rare:21 | ||||
| chr8:38562793-38562952 | Common:1; Rare:28 | ||||
| chr8:38720516-38720642 | Rare:23 | ||||
| chr8:38825227-38825373 | Rare:39 | ||||
| chr8:38843164-38843350 | Common:1; Rare:32 | ||||
| chr8:38867729-38867775 | Common:1; Rare:21 | ||||
| chr8:39180957-39181131 | Rare:31 | ||||
| chr8:39314568-39314662 | Common:1; Rare:24 | ||||
| chr8:39522820-39522928 | Common:1; Rare:22 | ||||
| chr8:39522934-39522984 | Rare:12 | ||||
| chr8:40903910-40904087 | Rare:27 |