Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:26382935-26383227 | Common:3; Rare:134 | ||||
chr8:26390246-26390492 | Common:1; Rare:47 | ||||
chr8:27311273-27311478 | Common:6; Rare:73 | ||||
chr8:28890179-28890431 | Rare:65 | ||||
chr8:30156219-30156386 | Common:1; Rare:52 | ||||
chr8:30156635-30156727 | Common:2; Rare:32 | ||||
chr8:31033617-31033905 | Common:4; Rare:68; Clinvar:5; Clinvar (benign):4 | ||||
chr8:33484952-33485204 | Common:7; Rare:86 | ||||
chr8:37762329-37762635 | Common:1; Rare:93 | ||||
chr8:38030290-38030632 | Common:3; Rare:102 | ||||
chr8:38105365-38105569 | Common:3; Rare:64 | ||||
chr8:38105755-38105929 | Rare:55 | ||||
chr8:38176441-38176535 | Common:1; Rare:34 | ||||
chr8:38176681-38176867 | Common:2; Rare:53 | ||||
chr8:38269158-38269249 | Rare:35 |