Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:40315335-40315601 | Common:4; Rare:65; Clinvar (benign):1 | ||||
chr1:40316640-40316828 | Common:1; Rare:46 | ||||
chr1:40373526-40373815 | Common:1; Rare:68 | ||||
chr1:40374266-40374866 | Common:13; Rare:112 | ||||
chr1:40449886-40450238 | Common:5; Rare:126 | ||||
chr1:40450249-40450499 | Common:3; Rare:60 | ||||
chr1:40477110-40477409 | Common:3; Rare:84 | ||||
chr1:40508416-40508446 | Rare:8 | ||||
chr1:40508547-40508807 | Common:6; Rare:69 | ||||
chr1:40531465-40531757 | Common:1; Rare:80 | ||||
chr1:40691475-40691796 | Common:3; Rare:154 | ||||
chr1:40691955-40692401 | Common:3; Rare:134 | ||||
chr1:40709117-40709371 | Rare:57 | ||||
chr1:40818680-40818732 | Common:1; Rare:29; Clinvar:1; Clinvar (benign):1 | ||||
chr1:40862335-40862610 | Common:5; Rare:92 |