Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:9997050-9997328 | Common:2; Rare:81 | ||||
chr1:10398857-10399125 | Common:2; Rare:105 | ||||
chr1:10430666-10430777 | Common:5; Rare:36 | ||||
chr1:10472375-10472657 | Rare:79 | ||||
chr1:11013048-11013276 | Common:1; Rare:76 | ||||
chr1:11099779-11099961 | Common:2; Rare:76 | ||||
chr1:11262484-11262817 | Common:2; Rare:104 | ||||
chr1:11273430-11273515 | Common:1; Rare:29; Clinvar (benign):1 | ||||
chr1:11654704-11654914 | Common:4; Rare:58 | ||||
chr1:11736020-11736196 | Common:3; Rare:52 | ||||
chr1:11805900-11806276 | Common:2; Rare:102; Clinvar:1 | ||||
chr1:11934553-11934771 | Common:3; Rare:71; Clinvar:5; Clinvar (benign):1 | ||||
chr1:11980161-11980499 | Common:5; Rare:111; Clinvar:1; Clinvar (benign):5 | ||||
chr1:12618202-12618464 | Common:1; Rare:58 | ||||
chr1:13700179-13700285 | Rare:44 |