Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:6602857-6603116 | Common:3; Rare:93 | ||||
chr1:7783984-7784344 | Common:1; Rare:149 | ||||
chr1:7961449-7961774 | Common:4; Rare:114; Clinvar:2; Clinvar (benign):3 | ||||
chr1:8422749-8422939 | Rare:46 | ||||
chr1:8423007-8423223 | Common:1; Rare:48 | ||||
chr1:8423427-8423490 | Rare:18 | ||||
chr1:8423499-8423576 | Rare:14 | ||||
chr1:8423639-8423913 | Common:1; Rare:116 | ||||
chr1:8424064-8424469 | Common:2; Rare:96 | ||||
chr1:8525837-8525999 | Rare:27 | ||||
chr1:8878578-8878835 | Rare:130 | ||||
chr1:9234672-9234993 | Common:6; Rare:136 | ||||
chr1:9239835-9239907 | Common:1; Rare:13 | ||||
chr1:9651641-9651792 | Common:3; Rare:36 | ||||
chr1:9943238-9943509 | Common:3; Rare:76 |