Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:63265202-63265330 | Rare:25 | ||||
chr10:69061836-69061871 | Rare:9 | ||||
chr10:70816572-70816751 | Rare:31 | ||||
chr10:71772155-71772444 | Common:2; Rare:51 | ||||
chr10:71825764-71825894 | Common:1; Rare:32; Clinvar (pathogenic):1 | ||||
chr10:71889079-71889219 | Common:3; Rare:28 | ||||
chr10:72260426-72260675 | Rare:50 | ||||
chr10:73126204-73126480 | Common:1; Rare:53 | ||||
chr10:73247208-73247371 | Rare:89 | ||||
chr10:73730456-73730796 | Common:1; Rare:72 | ||||
chr10:73790272-73790437 | Rare:28 | ||||
chr10:75230787-75231049 | Common:2; Rare:59 | ||||
chr10:75403388-75403465 | Rare:14 | ||||
chr10:75403496-75403928 | Common:2; Rare:102 | ||||
chr10:75409572-75409729 | Common:3; Rare:39 |