Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:7961452-7961793 | Common:4; Rare:117; Clinvar:3; Clinvar (benign):3 | ||||
chr1:8026177-8026459 | Common:2; Rare:129 | ||||
chr1:8318025-8318154 | Rare:41 | ||||
chr1:8422967-8423019 | Rare:6 | ||||
chr1:8423562-8423724 | Common:1; Rare:46 | ||||
chr1:8424080-8424518 | Common:3; Rare:107 | ||||
chr1:8878578-8878842 | Rare:136 | ||||
chr1:9239610-9239766 | Rare:39 | ||||
chr1:9239778-9239903 | Common:2; Rare:24 | ||||
chr1:9733532-9733815 | Common:1; Rare:78 | ||||
chr1:9943051-9943500 | Common:6; Rare:115 | ||||
chr1:9997156-9997260 | Common:1; Rare:37 | ||||
chr1:10032763-10033099 | Common:2; Rare:87 | ||||
chr1:10365180-10365487 | Common:1; Rare:88; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:10398837-10399125 | Common:2; Rare:115 |