Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:96053374-96053585 | Common:2; Rare:83 | ||||
chr13:99200668-99200886 | Common:6; Rare:98 | ||||
chr13:100088929-100089117 | Rare:67; Clinvar:1; Clinvar (benign):2 | ||||
chr13:102596807-102597035 | Common:1; Rare:109 | ||||
chr13:102773736-102773843 | Rare:52 | ||||
chr13:108218350-108218520 | Rare:69 | ||||
chr13:111153619-111153695 | Common:2; Rare:26 | ||||
chr13:113208632-113208723 | Rare:53 | ||||
chr13:114281505-114281611 | Common:1; Rare:50 | ||||
chr14:20343252-20343635 | Common:11; Rare:220 | ||||
chr14:20684461-20684595 | Common:1; Rare:21; Clinvar (benign):1 | ||||
chr14:21456058-21456235 | Common:2; Rare:53 | ||||
chr14:21476942-21477253 | Rare:86 | ||||
chr14:22982504-22982736 | Rare:88 | ||||
chr14:23095108-23095334 | Common:1; Rare:121 |