Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:74176641-74176806 | Rare:47; Clinvar:3 | ||||
chr10:74825290-74825616 | Rare:84 | ||||
chr10:75210443-75210607 | Rare:53 | ||||
chr10:75210742-75210935 | Common:2; Rare:76 | ||||
chr10:75401780-75401920 | Common:2; Rare:47 | ||||
chr10:75402312-75402424 | Common:1; Rare:36 | ||||
chr10:78029484-78029733 | Common:3; Rare:57; Clinvar (benign):1 | ||||
chr10:79445203-79445504 | Common:1; Rare:64 | ||||
chr10:80078614-80078706 | Rare:36 | ||||
chr10:80079179-80079286 | Common:1; Rare:45 | ||||
chr10:80132573-80132790 | Rare:62 | ||||
chr10:80205413-80205648 | Common:4; Rare:78 | ||||
chr10:80408437-80408623 | Common:1; Rare:57 | ||||
chr10:86521749-86521962 | Rare:69 | ||||
chr10:86668292-86668575 | Common:5; Rare:68; Clinvar (benign):3 |