Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:58347540-58347780 | Common:8; Rare:108 | ||||
chr19:58386719-58386810 | Common:2; Rare:26 | ||||
chr19:58408452-58408686 | Common:3; Rare:71 | ||||
chr19:58440136-58440448 | Common:6; Rare:82 | ||||
chr19:58499192-58499526 | Common:3; Rare:103; Clinvar:3; Clinvar (benign):1 | ||||
chr19:58519787-58520030 | Rare:69 | ||||
chr19:58554919-58555262 | Common:2; Rare:120 | ||||
chr19:58558310-58558656 | Rare:108 | ||||
chr2:677349-677723 | Common:3; Rare:130 | ||||
chr2:3377785-3377953 | Rare:46 | ||||
chr2:3379611-3379729 | Common:1; Rare:39 | ||||
chr2:3519483-3519660 | Common:2; Rare:55 | ||||
chr2:3558251-3558658 | Common:6; Rare:150 | ||||
chr2:3575098-3575447 | Common:2; Rare:98; Clinvar:3; Clinvar (benign):6 | ||||
chr2:9423148-9423270 | Common:1; Rare:26 |