Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:117605792-117606090 | Rare:94 | ||||
chr1:117929546-117929800 | Common:2; Rare:75 | ||||
chr1:119140640-119140776 | Common:1; Rare:43 | ||||
chr1:119648131-119648364 | Common:3; Rare:81 | ||||
chr1:120069594-120069864 | Common:7; Rare:62 | ||||
chr1:145607875-145608069 | Common:2; Rare:60 | ||||
chr1:145823869-145824249 | Rare:132 | ||||
chr1:145918680-145919022 | Common:2; Rare:79 | ||||
chr1:145927400-145927644 | Common:1; Rare:67; Clinvar (pathogenic):1 | ||||
chr1:145964571-145964742 | Rare:45 | ||||
chr1:145996455-145996882 | Common:2; Rare:166 | ||||
chr1:147172142-147172284 | Rare:35 | ||||
chr1:147172420-147172823 | Common:1; Rare:103 | ||||
chr1:147224989-147225197 | Rare:56 | ||||
chr1:147225238-147225430 | Common:2; Rare:38 |