Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:38996261-38996336 | Common:1; Rare:43 | ||||
chr8:38996449-38997038 | Common:7; Rare:222 | ||||
chr8:41578434-41578556 | Rare:32 | ||||
chr8:42155684-42155914 | Common:2; Rare:38 | ||||
chr8:42541557-42541598 | Rare:8 | ||||
chr8:42541628-42541670 | Rare:17 | ||||
chr8:42541700-42541811 | Rare:46 | ||||
chr8:42541907-42542111 | Common:1; Rare:52; Clinvar:3; Clinvar (benign):1 | ||||
chr8:42896555-42897037 | Common:1; Rare:195 | ||||
chr8:43056089-43056454 | Common:1; Rare:128 | ||||
chr8:43093411-43093555 | Common:3; Rare:29; Clinvar (benign):1 | ||||
chr8:43140309-43140468 | Common:2; Rare:67; Clinvar:4 | ||||
chr8:47960136-47960256 | Common:1; Rare:34; Clinvar (benign):1 | ||||
chr8:51899049-51899246 | Common:4; Rare:93 | ||||
chr8:52714400-52714587 | Common:1; Rare:85 |