Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:182391279-182391530 | Common:1; Rare:62 | ||||
chr1:182391717-182392077 | Common:4; Rare:136; Clinvar:6; Clinvar (benign):4 | ||||
chr1:182392165-182392308 | Common:2; Rare:37; Clinvar (benign):1 | ||||
chr1:182588819-182588923 | Common:1; Rare:22 | ||||
chr1:182588992-182589038 | Common:2; Rare:7 | ||||
chr1:182589160-182589320 | Rare:33 | ||||
chr1:182604338-182604573 | Rare:57 | ||||
chr1:182789578-182789829 | Common:2; Rare:87 | ||||
chr1:182839185-182839454 | Common:1; Rare:110 | ||||
chr1:182839529-182839813 | Common:2; Rare:118 | ||||
chr1:182839949-182840374 | Common:2; Rare:108 | ||||
chr1:183022943-183023637 | Common:7; Rare:186 | ||||
chr1:183023832-183024163 | Common:1; Rare:98 | ||||
chr1:183185950-183186483 | Common:6; Rare:138; Clinvar:6; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr1:183418319-183418494 | Rare:39 |