Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:102845657-102846161 | Common:9; Rare:131; Clinvar:4; Clinvar (benign):4 | ||||
chr13:108218313-108218512 | Rare:75 | ||||
chr13:110307155-110307500 | Common:5; Rare:105; Clinvar (benign):6 | ||||
chr13:110615503-110615581 | Rare:23 | ||||
chr13:110713023-110713266 | Common:2; Rare:105 | ||||
chr13:111153557-111153718 | Common:2; Rare:78 | ||||
chr13:113208632-113208741 | Rare:63 | ||||
chr14:20343219-20343637 | Common:12; Rare:239 | ||||
chr14:20413422-20413531 | Common:3; Rare:30 | ||||
chr14:20455078-20455287 | Common:2; Rare:67 | ||||
chr14:20684428-20684686 | Common:2; Rare:45; Clinvar:1; Clinvar (benign):2 | ||||
chr14:21022141-21022443 | Rare:77 | ||||
chr14:21476909-21477267 | Common:1; Rare:105 | ||||
chr14:21511327-21511549 | Rare:54 | ||||
chr14:22766557-22766719 | Common:1; Rare:89 |