Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:48306894-48307015 | Rare:38 | ||||
chr10:48307025-48307169 | Common:2; Rare:40 | ||||
chr10:48604653-48604747 | Rare:25 | ||||
chr10:48604891-48605241 | Common:1; Rare:81 | ||||
chr10:48656212-48656533 | Common:4; Rare:78 | ||||
chr10:49538713-49538903 | Common:7; Rare:52 | ||||
chr10:49538957-49539399 | Common:4; Rare:129; Clinvar:3; Clinvar (benign):3 | ||||
chr10:49539447-49539486 | Rare:8 | ||||
chr10:49539513-49539693 | Common:1; Rare:32 | ||||
chr10:49941909-49942083 | Rare:49 | ||||
chr10:50067410-50067664 | Common:1; Rare:38 | ||||
chr10:50067720-50068015 | Common:6; Rare:111 | ||||
chr10:50418002-50418222 | Common:1; Rare:55 | ||||
chr10:50418254-50418595 | Rare:77 | ||||
chr10:50623345-50623747 | Common:2; Rare:94 |