Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:58362528-58362623 | Rare:31 | ||||
chr19:58401244-58401538 | Common:5; Rare:90 | ||||
chr19:58408449-58408685 | Common:3; Rare:74 | ||||
chr19:58499222-58499545 | Common:2; Rare:104; Clinvar:3; Clinvar (benign):1 | ||||
chr19:58554943-58555210 | Common:2; Rare:84 | ||||
chr2:676320-676468 | Common:2; Rare:33 | ||||
chr2:677342-677564 | Common:1; Rare:95 | ||||
chr2:3377796-3377953 | Rare:41 | ||||
chr2:3519516-3519680 | Common:2; Rare:41 | ||||
chr2:3558263-3558509 | Common:5; Rare:105 | ||||
chr2:3575120-3575358 | Common:2; Rare:69; Clinvar:3; Clinvar (benign):5 | ||||
chr2:9423457-9423731 | Rare:91 | ||||
chr2:9474504-9474575 | Common:6; Rare:43 | ||||
chr2:9555719-9555966 | Common:2; Rare:84 | ||||
chr2:9843395-9843553 | Common:5; Rare:43 |