Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:52314101-52314284 | Common:1; Rare:43 | ||||
chr10:56361215-56361520 | Common:7; Rare:112 | ||||
chr10:60944146-60944353 | Common:1; Rare:72 | ||||
chr10:68332926-68333044 | Rare:28 | ||||
chr10:71819465-71819896 | Common:1; Rare:172; Clinvar:5; Clinvar (benign):4 | ||||
chr10:71851183-71851453 | Common:5; Rare:115; Clinvar:4; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
chr10:72273664-72273970 | Rare:90 | ||||
chr10:72626094-72626313 | Common:1; Rare:57 | ||||
chr10:73167934-73168167 | Rare:62 | ||||
chr10:73252611-73252808 | Rare:53; Clinvar:3 | ||||
chr10:73495618-73495755 | Rare:26 | ||||
chr10:73744256-73744419 | Common:1; Rare:42 | ||||
chr10:73781946-73782078 | Common:1; Rare:40 | ||||
chr10:74150765-74151270 | Common:2; Rare:123 | ||||
chr10:75401762-75401887 | Common:1; Rare:35 |