Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:17230021-17230140 | Common:2; Rare:37 | ||||
chr10:17233583-17233930 | Common:3; Rare:110; Clinvar (benign):1 | ||||
chr10:17643869-17644318 | Common:2; Rare:140 | ||||
chr10:18659265-18659484 | Common:2; Rare:78 | ||||
chr10:25016444-25016658 | Common:6; Rare:79 | ||||
chr10:27154183-27154511 | Rare:96 | ||||
chr10:28532650-28532779 | Common:1; Rare:53 | ||||
chr10:28533021-28533194 | Rare:70 | ||||
chr10:31318631-31318914 | Common:1; Rare:82 | ||||
chr10:31318976-31319240 | Common:2; Rare:77 | ||||
chr10:31928792-31928927 | Common:2; Rare:51 | ||||
chr10:32957809-32958101 | Common:5; Rare:94 | ||||
chr10:35127142-35127229 | Rare:18 | ||||
chr10:43138346-43138557 | Common:2; Rare:82 | ||||
chr10:43436706-43436908 | Common:4; Rare:79 |