Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:128059821-128059939 | Common:2; Rare:14 | ||||
chr10:130110479-130110555 | Common:1; Rare:25 | ||||
chr10:130110790-130110932 | Rare:46 | ||||
chr10:131947331-131947634 | Rare:56 | ||||
chr10:131970898-131971078 | Rare:44 | ||||
chr10:132408458-132408618 | Rare:40 | ||||
chr10:133235402-133235524 | Common:1; Rare:26 | ||||
chr10:133293224-133293427 | Rare:47 | ||||
chr10:133294706-133294983 | Rare:53 | ||||
chr11:287995-288217 | Common:4; Rare:41 | ||||
chr11:318525-318680 | Rare:9 | ||||
chr11:319540-319757 | Common:1; Rare:55 | ||||
chr11:319848-320149 | Common:1; Rare:89 | ||||
chr11:532705-532826 | Common:1; Rare:44; Clinvar:7; Clinvar (benign):5 | ||||
chr11:758908-759002 | Common:1; Rare:27 |