Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:47798481-47798685 | Common:2; Rare:78; Clinvar:21; Clinvar (benign):15; Clinvar (pathogenic):2 | ||||
chr2:47906417-47906900 | Common:2; Rare:177 | ||||
chr2:54560438-54560604 | Common:2; Rare:50 | ||||
chr2:54618071-54618430 | Common:5; Rare:83 | ||||
chr2:55282245-55282381 | Common:5; Rare:46 | ||||
chr2:56185770-56186009 | Common:2; Rare:69 | ||||
chr2:61190311-61190498 | Common:1; Rare:55 | ||||
chr2:64453195-64453454 | Common:3; Rare:38 | ||||
chr2:64645180-64645303 | Common:2; Rare:31 | ||||
chr2:65020850-65020943 | Rare:31; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr2:65204678-65204992 | Rare:59 | ||||
chr2:65435762-65435950 | Common:2; Rare:52 | ||||
chr2:66446338-66446513 | Common:1; Rare:54 | ||||
chr2:66575351-66575468 | Common:8; Rare:33 | ||||
chr2:66578367-66578523 | Rare:24 |