Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:156751847-156751963 | Rare:32 | ||||
chr1:156766880-156767208 | Rare:55 | ||||
chr1:156767367-156767574 | Common:1; Rare:70 | ||||
chr1:157138331-157138632 | Common:3; Rare:88 | ||||
chr1:159924524-159924725 | Rare:53 | ||||
chr1:159925460-159925617 | Common:1; Rare:42 | ||||
chr1:160262433-160262627 | Common:1; Rare:60 | ||||
chr1:160285077-160285170 | Common:2; Rare:41; Clinvar:2; Clinvar (benign):4 | ||||
chr1:160343181-160343400 | Rare:90 | ||||
chr1:161045888-161046052 | Common:1; Rare:43 | ||||
chr1:161118000-161118141 | Rare:73 | ||||
chr1:161132417-161132698 | Common:1; Rare:93 | ||||
chr1:161159396-161159529 | Common:1; Rare:36 | ||||
chr1:161166263-161166511 | Common:2; Rare:60; Clinvar:3; Clinvar (benign):1 | ||||
chr1:161197216-161197419 | Common:2; Rare:35 |