Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:110500848-110501042 | Common:1; Rare:38 | ||||
chr10:110501869-110502039 | Common:1; Rare:41 | ||||
chr10:110503258-110503564 | Common:3; Rare:48 | ||||
chr10:110596469-110596613 | Common:1; Rare:40; Clinvar (benign):2 | ||||
chr10:110873784-110874093 | Common:1; Rare:52 | ||||
chr10:110879233-110879349 | Common:1; Rare:15 | ||||
chr10:110879502-110879786 | Common:1; Rare:52 | ||||
chr10:110883003-110883472 | Common:3; Rare:76 | ||||
chr10:110902605-110902922 | Rare:63 | ||||
chr10:110911568-110911610 | Rare:8 | ||||
chr10:110917612-110917867 | Common:2; Rare:53 | ||||
chr10:110947537-110947639 | Rare:22 | ||||
chr10:110955367-110955491 | Common:1; Rare:20 | ||||
chr10:110998325-110998377 | Common:1; Rare:7 | ||||
chr10:111022474-111022614 | Common:1; Rare:25 |