Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:22714193-22714237 | Rare:14 | ||||
chr10:23095336-23095616 | Rare:53 | ||||
chr10:23438803-23439150 | Common:5; Rare:142 | ||||
chr10:23439346-23439478 | Common:1; Rare:44 | ||||
chr10:24466323-24466709 | Common:2; Rare:60 | ||||
chr10:24594940-24595148 | Common:2; Rare:48 | ||||
chr10:25016344-25016726 | Common:10; Rare:143 | ||||
chr10:26860797-26861076 | Common:2; Rare:96 | ||||
chr10:27154178-27154554 | Rare:107 | ||||
chr10:27155146-27155374 | Common:3; Rare:73; Clinvar:5; Clinvar (benign):3 | ||||
chr10:27240767-27241095 | Common:3; Rare:70 | ||||
chr10:27242079-27242211 | Common:1; Rare:56 | ||||
chr10:27504023-27504409 | Rare:165; Clinvar:5; Clinvar (benign):1 | ||||
chr10:28532612-28532886 | Common:1; Rare:111 | ||||
chr10:28532938-28533303 | Common:1; Rare:150 |