Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:10448297-10448737 | Common:1; Rare:139 | ||||
chr2:10689925-10689997 | Common:2; Rare:22 | ||||
chr2:11746369-11746674 | Common:2; Rare:86; Clinvar:4 | ||||
chr2:17753750-17754168 | Common:4; Rare:131; Clinvar (benign):1 | ||||
chr2:19358602-19358758 | Rare:38 | ||||
chr2:20051524-20051836 | Common:1; Rare:88 | ||||
chr2:20651040-20651260 | Rare:68 | ||||
chr2:24076297-24076520 | Rare:61 | ||||
chr2:24084770-24084959 | Common:3; Rare:28 | ||||
chr2:24793133-24793464 | Rare:144; Clinvar:1 | ||||
chr2:24971936-24972143 | Common:1; Rare:58 | ||||
chr2:26033805-26034194 | Common:2; Rare:132 | ||||
chr2:26244594-26244967 | Common:2; Rare:136; Clinvar:5; Clinvar (benign):8 | ||||
chr2:26345785-26346172 | Common:1; Rare:117 | ||||
chr2:27032821-27033052 | Rare:87 |