Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:89632918-89633196 | Common:1; Rare:79 | ||||
chr1:89820908-89821289 | Common:1; Rare:113 | ||||
chr1:89821782-89822048 | Common:1; Rare:70 | ||||
chr1:89994973-89995241 | Common:2; Rare:102 | ||||
chr1:91021967-91022311 | Rare:95 | ||||
chr1:91500568-91500895 | Common:3; Rare:80 | ||||
chr1:91885988-91886340 | Rare:144 | ||||
chr1:92298945-92299076 | Common:1; Rare:66; Clinvar:1; Clinvar (benign):1 | ||||
chr1:92483615-92483932 | Common:2; Rare:69 | ||||
chr1:92831996-92832113 | Rare:76; Clinvar:6; Clinvar (benign):5 | ||||
chr1:92961430-92961804 | Common:3; Rare:113 | ||||
chr1:93079069-93079337 | Common:4; Rare:112 | ||||
chr1:93179665-93179961 | Common:1; Rare:59 | ||||
chr1:93180049-93180108 | Rare:21 | ||||
chr1:93180110-93180754 | Common:2; Rare:249 |