Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:154956085-154956215 | Rare:37 | ||||
chr1:154961476-154961560 | Rare:24 | ||||
chr1:154961717-154962037 | Common:1; Rare:111 | ||||
chr1:154970124-154970487 | Common:1; Rare:115 | ||||
chr1:154970703-154970844 | Rare:28 | ||||
chr1:154974322-154974768 | Rare:116 | ||||
chr1:154983070-154983402 | Common:2; Rare:66; Clinvar (benign):1 | ||||
chr1:155051144-155051381 | Common:2; Rare:81 | ||||
chr1:155085404-155085518 | Common:1; Rare:28 | ||||
chr1:155127202-155127471 | Common:1; Rare:53 | ||||
chr1:155127751-155127937 | Common:1; Rare:40 | ||||
chr1:155135700-155135920 | Common:3; Rare:96 | ||||
chr1:155140499-155140596 | Common:1; Rare:30 | ||||
chr1:155173160-155173387 | Common:3; Rare:105 | ||||
chr1:155173817-155173876 | Rare:12 |