Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:154956085-154956240 | Common:1; Rare:44 | ||||
chr1:154961483-154961568 | Rare:26 | ||||
chr1:154970076-154970337 | Common:1; Rare:79 | ||||
chr1:154970494-154970543 | Rare:18 | ||||
chr1:154970629-154970852 | Rare:38 | ||||
chr1:154974322-154974802 | Rare:122 | ||||
chr1:154982900-154983400 | Common:3; Rare:98; Clinvar (benign):1 | ||||
chr1:155051118-155051449 | Common:2; Rare:114 | ||||
chr1:155127722-155127945 | Common:1; Rare:50 | ||||
chr1:155135687-155135892 | Common:3; Rare:89 | ||||
chr1:155136161-155136323 | Common:3; Rare:47 | ||||
chr1:155173212-155173428 | Common:2; Rare:92 | ||||
chr1:155209131-155209266 | Rare:61 | ||||
chr1:155244557-155244917 | Common:3; Rare:94 | ||||
chr1:155255393-155255608 | Common:2; Rare:43 |