Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:26991845-26992013 | Rare:32 | ||||
chr2:27025443-27025936 | Common:2; Rare:113 | ||||
chr2:27493392-27493702 | Common:1; Rare:68 | ||||
chr2:27655508-27655871 | Common:3; Rare:80 | ||||
chr2:27735605-27735825 | Common:1; Rare:49 | ||||
chr2:27738558-27738689 | Rare:19 | ||||
chr2:27774278-27774455 | Common:1; Rare:45 | ||||
chr2:31729204-31729339 | Common:3; Rare:27 | ||||
chr2:42325413-42325532 | Common:1; Rare:28 | ||||
chr2:42328808-42328950 | Common:1; Rare:44 | ||||
chr2:46004038-46004250 | Common:1; Rare:50 | ||||
chr2:46006739-46006990 | Common:3; Rare:65 | ||||
chr2:47795629-47795995 | Common:4; Rare:97; Clinvar:18; Clinvar (benign):11; Clinvar (pathogenic):2 | ||||
chr2:47804787-47805022 | Common:1; Rare:100; Clinvar:25; Clinvar (benign):13; Clinvar (pathogenic):7 | ||||
chr2:47906435-47906817 | Common:2; Rare:147 |