Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:26697097-26697228 | Rare:27 | ||||
chr10:26697299-26697470 | Common:3; Rare:41 | ||||
chr10:26697498-26697751 | Common:1; Rare:73; Clinvar (benign):1 | ||||
chr10:26697778-26698035 | Common:3; Rare:71; Clinvar:2; Clinvar (benign):2 | ||||
chr10:26860054-26860377 | Common:1; Rare:83 | ||||
chr10:26860500-26861082 | Common:4; Rare:162 | ||||
chr10:27100129-27100285 | Common:1; Rare:81; Clinvar:6; Clinvar (benign):2 | ||||
chr10:27100357-27100672 | Common:5; Rare:82; Clinvar:4; Clinvar (benign):3 | ||||
chr10:27153889-27154208 | Common:5; Rare:82 | ||||
chr10:27154243-27154546 | Rare:85 | ||||
chr10:27154906-27155050 | Common:1; Rare:29; Clinvar (benign):1 | ||||
chr10:27155071-27155435 | Common:7; Rare:135; Clinvar:7; Clinvar (benign):7 | ||||
chr10:27155726-27155761 | Rare:6 | ||||
chr10:27240310-27240729 | Common:2; Rare:123 | ||||
chr10:27240746-27240856 | Rare:32 |