Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:99307337-99307632 | Common:2; Rare:44 | ||||
chr13:99312543-99312830 | Rare:44 | ||||
chr13:100088954-100089128 | Rare:64; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr13:102596773-102597021 | Common:1; Rare:110 | ||||
chr13:106568105-106568258 | Rare:49 | ||||
chr13:108215502-108215581 | Rare:22 | ||||
chr13:108218318-108218494 | Rare:66 | ||||
chr13:108269999-108270036 | Rare:11 | ||||
chr13:110561632-110561923 | Common:5; Rare:98 | ||||
chr13:110715829-110715892 | Rare:43 | ||||
chr13:110915016-110915296 | Common:3; Rare:109 | ||||
chr13:112689724-112690073 | Common:6; Rare:107 | ||||
chr13:113208623-113208749 | Rare:75 | ||||
chr13:113490687-113490995 | Common:1; Rare:113 | ||||
chr13:114234992-114235124 | Common:3; Rare:40 |