Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:26218490-26218605 | Common:5; Rare:30 | ||||
chr10:26697570-26697975 | Common:3; Rare:116; Clinvar:2; Clinvar (benign):3 | ||||
chr10:26860848-26861247 | Common:5; Rare:118 | ||||
chr10:27100403-27100587 | Common:3; Rare:56; Clinvar:4; Clinvar (benign):2 | ||||
chr10:27154239-27154521 | Rare:81 | ||||
chr10:27155161-27155376 | Common:4; Rare:70; Clinvar:5; Clinvar (benign):4 | ||||
chr10:27240485-27240560 | Rare:33 | ||||
chr10:27240570-27240637 | Common:2; Rare:17 | ||||
chr10:27240691-27240896 | Rare:55 | ||||
chr10:27241864-27241972 | Common:1; Rare:24 | ||||
chr10:27242079-27242255 | Common:1; Rare:78 | ||||
chr10:27242311-27242405 | Common:1; Rare:23 | ||||
chr10:27504031-27504372 | Rare:152; Clinvar:4; Clinvar (benign):1 | ||||
chr10:28532455-28532873 | Common:5; Rare:157 | ||||
chr10:28533002-28533197 | Rare:78 |