| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:42391697-42391928 | Common:3; Rare:82 | ||||
| chr8:42540946-42541178 | Rare:61 | ||||
| chr8:42541555-42541671 | Rare:39 | ||||
| chr8:42541674-42542052 | Common:1; Rare:118; Clinvar:3; Clinvar (benign):1 | ||||
| chr8:42843045-42843092 | Rare:11; Clinvar:2 | ||||
| chr8:42843277-42843591 | Common:3; Rare:83; Clinvar (benign):3 | ||||
| chr8:42896298-42896480 | Common:2; Rare:101 | ||||
| chr8:42896568-42897027 | Common:1; Rare:184 | ||||
| chr8:42897266-42897405 | Rare:39 | ||||
| chr8:43056196-43056463 | Rare:106 | ||||
| chr8:43140391-43140535 | Common:1; Rare:56; Clinvar:5 | ||||
| chr8:47260803-47260981 | Common:3; Rare:74 | ||||
| chr8:47960046-47960273 | Common:2; Rare:85; Clinvar:2; Clinvar (benign):3 | ||||
| chr8:47960676-47961079 | Common:2; Rare:149; Clinvar:10; Clinvar (benign):1 | ||||
| chr8:48008348-48008467 | Common:2; Rare:71 |