| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:38268886-38269313 | Rare:161 | ||||
| chr8:38381810-38381931 | Rare:23 | ||||
| chr8:38382143-38382410 | Common:2; Rare:82 | ||||
| chr8:38386357-38386527 | Rare:36 | ||||
| chr8:38404165-38404345 | Rare:48 | ||||
| chr8:38466143-38466329 | Common:2; Rare:54 | ||||
| chr8:38467607-38467734 | Common:2; Rare:26 | ||||
| chr8:38786988-38787279 | Rare:110 | ||||
| chr8:38901020-38901360 | Common:2; Rare:79 | ||||
| chr8:38950765-38950974 | Rare:70 | ||||
| chr8:38996248-38996345 | Common:1; Rare:51 | ||||
| chr8:38996425-38997157 | Common:8; Rare:273; Clinvar (benign):1 | ||||
| chr8:40153341-40153541 | Common:1; Rare:50 | ||||
| chr8:41308858-41309115 | Common:1; Rare:77 | ||||
| chr8:41309171-41309378 | Common:1; Rare:49 |