Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:99905434-99905733 | Common:2; Rare:43 | ||||
chr10:99923665-99923912 | Common:3; Rare:42 | ||||
chr10:99927022-99927302 | Common:2; Rare:51 | ||||
chr10:99930792-99931029 | Common:2; Rare:61 | ||||
chr10:100236169-100236173 | |||||
chr10:100970112-100970382 | Rare:68 | ||||
chr10:100979618-100979882 | Common:1; Rare:64 | ||||
chr10:101032195-101032457 | Common:3; Rare:61 | ||||
chr10:101694404-101694693 | Common:4; Rare:93; Clinvar:3; Clinvar (benign):5 | ||||
chr10:102109451-102109605 | Common:1; Rare:31 | ||||
chr10:102363067-102363322 | Common:1; Rare:61 | ||||
chr10:102919642-102920095 | Rare:82; Clinvar:1 | ||||
chr10:103090721-103091040 | Common:5; Rare:86; Clinvar (pathogenic):1 | ||||
chr10:103097296-103097647 | Common:3; Rare:64 | ||||
chr10:103192445-103192679 | Rare:59 |