Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:97334701-97334843 | Common:1; Rare:57 | ||||
chr10:97426035-97426300 | Common:2; Rare:116 | ||||
chr10:97445928-97446239 | Common:1; Rare:90 | ||||
chr10:97497790-97497896 | Rare:19 | ||||
chr10:97498380-97498532 | Common:1; Rare:67 | ||||
chr10:97633413-97633696 | Common:2; Rare:78 | ||||
chr10:97687271-97687467 | Common:3; Rare:66 | ||||
chr10:97736936-97737220 | Common:2; Rare:99 | ||||
chr10:97849772-97849843 | Rare:13 | ||||
chr10:98134529-98134703 | Common:1; Rare:64 | ||||
chr10:98134731-98134916 | Common:1; Rare:52 | ||||
chr10:99430616-99430986 | Common:3; Rare:90 | ||||
chr10:99659221-99659361 | Common:1; Rare:31 | ||||
chr10:99659371-99659536 | Rare:46 | ||||
chr10:99732027-99732332 | Rare:113; Clinvar:4; Clinvar (benign):1 |