Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:7771127-7771316 | Common:4; Rare:73 | ||||
chr1:7961455-7961779 | Common:4; Rare:109; Clinvar:2; Clinvar (benign):3 | ||||
chr1:8878582-8878880 | Rare:159 | ||||
chr1:9943288-9943492 | Common:2; Rare:50 | ||||
chr1:10398827-10399114 | Common:2; Rare:114 | ||||
chr1:10430667-10430796 | Common:5; Rare:40 | ||||
chr1:10472479-10472678 | Rare:41 | ||||
chr1:11012700-11012734 | Rare:7; Clinvar:1 | ||||
chr1:11060042-11060349 | Common:3; Rare:96 | ||||
chr1:11099827-11099939 | Common:2; Rare:40 | ||||
chr1:11654826-11654888 | Common:1; Rare:16 | ||||
chr1:11805905-11806227 | Common:2; Rare:87; Clinvar:1 | ||||
chr1:15409800-15409971 | Rare:57 | ||||
chr1:15410056-15410251 | Common:2; Rare:64 | ||||
chr1:15526532-15526897 | Common:2; Rare:116 |