Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:22321054-22321221 | Common:1; Rare:42 | ||||
chr10:22321348-22321590 | Rare:88 | ||||
chr10:22714507-22714680 | Rare:69 | ||||
chr10:23438772-23439106 | Common:5; Rare:131 | ||||
chr10:26697522-26697744 | Common:1; Rare:65; Clinvar (benign):1 | ||||
chr10:27100419-27100587 | Common:3; Rare:51; Clinvar:4; Clinvar (benign):2 | ||||
chr10:27154178-27154521 | Rare:100 | ||||
chr10:27155146-27155371 | Common:3; Rare:73; Clinvar:5; Clinvar (benign):3 | ||||
chr10:27240478-27240652 | Common:2; Rare:56 | ||||
chr10:27242059-27242198 | Common:1; Rare:59 | ||||
chr10:27504066-27504413 | Rare:158; Clinvar:5; Clinvar (benign):1 | ||||
chr10:28532524-28532862 | Common:4; Rare:141 | ||||
chr10:28532953-28533538 | Common:1; Rare:230 | ||||
chr10:28533716-28534032 | Common:4; Rare:124 | ||||
chr10:30349309-30349438 | Common:9; Rare:35 |