| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:38231510-38231781 | Rare:76 | ||||
| chr8:38901691-38901851 | Common:3; Rare:28 | ||||
| chr8:38996443-38997038 | Common:7; Rare:225 | ||||
| chr8:39948873-39949133 | Common:1; Rare:52 | ||||
| chr8:40153049-40153176 | Common:1; Rare:29 | ||||
| chr8:40153341-40153546 | Common:1; Rare:53 | ||||
| chr8:41577946-41578256 | Rare:98 | ||||
| chr8:41578406-41578528 | Rare:34 | ||||
| chr8:41797500-41797878 | Common:2; Rare:106; Clinvar (pathogenic):2 | ||||
| chr8:42391751-42391925 | Common:1; Rare:62 | ||||
| chr8:42541016-42541182 | Rare:43 | ||||
| chr8:42541494-42541872 | Common:3; Rare:126; Clinvar (benign):1 | ||||
| chr8:42843045-42843113 | Rare:19; Clinvar:3 | ||||
| chr8:42843290-42843457 | Common:2; Rare:42; Clinvar (benign):3 | ||||
| chr8:42896302-42896451 | Common:1; Rare:71 |