Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:71819465-71819902 | Common:1; Rare:172; Clinvar:5; Clinvar (benign):4 | ||||
chr10:71851183-71851427 | Common:5; Rare:106; Clinvar:4; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
chr10:72216237-72216344 | Rare:48 | ||||
chr10:72273587-72274069 | Rare:137 | ||||
chr10:72354890-72355199 | Common:2; Rare:111 | ||||
chr10:72626047-72626309 | Common:1; Rare:64 | ||||
chr10:72868582-72868828 | Rare:45 | ||||
chr10:73096748-73097035 | Common:4; Rare:85 | ||||
chr10:73167903-73168337 | Rare:119 | ||||
chr10:73252525-73252867 | Common:2; Rare:98; Clinvar:5; Clinvar (benign):2 | ||||
chr10:73413963-73414199 | Common:3; Rare:69 | ||||
chr10:73495593-73495775 | Rare:41 | ||||
chr10:73495798-73496134 | Common:2; Rare:91 | ||||
chr10:73591293-73591477 | Common:1; Rare:42 | ||||
chr10:73592024-73592168 | Rare:29 |