Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:42896627-42897027 | Common:1; Rare:161 | ||||
chr8:43056196-43056454 | Rare:105 | ||||
chr8:47960122-47960199 | Rare:25; Clinvar (benign):1 | ||||
chr8:47960683-47961031 | Common:2; Rare:134; Clinvar:10; Clinvar (benign):1 | ||||
chr8:51899001-51899334 | Common:7; Rare:149 | ||||
chr8:52714383-52714613 | Common:1; Rare:102 | ||||
chr8:53843254-53843354 | Rare:20 | ||||
chr8:55773371-55773497 | Common:3; Rare:43 | ||||
chr8:56074417-56074617 | Common:3; Rare:97 | ||||
chr8:59119106-59119273 | Rare:46 | ||||
chr8:60516777-60517217 | Common:3; Rare:150 | ||||
chr8:63038743-63038919 | Common:3; Rare:69 | ||||
chr8:63168445-63168662 | Common:2; Rare:72 | ||||
chr8:65634130-65634405 | Common:3; Rare:72 | ||||
chr8:66667162-66667400 | Common:2; Rare:70 |