Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:58269919-58270147 | Common:2; Rare:41 | ||||
chr10:63496682-63496910 | Rare:42 | ||||
chr10:68292143-68292442 | Common:1; Rare:74 | ||||
chr10:69232838-69233127 | Common:4; Rare:99 | ||||
chr10:71764105-71764166 | Rare:6 | ||||
chr10:71772481-71772797 | Common:1; Rare:50 | ||||
chr10:71817351-71817658 | Common:1; Rare:85; Clinvar:1; Clinvar (benign):2 | ||||
chr10:73126205-73126357 | Common:1; Rare:32 | ||||
chr10:73246779-73246921 | Rare:59 | ||||
chr10:73247166-73247382 | Rare:119 | ||||
chr10:73730452-73730584 | Common:1; Rare:36 | ||||
chr10:73824278-73824404 | Rare:23 | ||||
chr10:73830048-73830092 | Rare:11 | ||||
chr10:74070784-74071050 | Rare:55; Clinvar:1; Clinvar (benign):5 | ||||
chr10:74107016-74107270 | Common:1; Rare:52; Clinvar:4; Clinvar (benign):1 |