Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:100376259-100376495 | Common:3; Rare:77 | ||||
chr14:101964328-101964622 | Common:3; Rare:90; Clinvar:1 | ||||
chr14:102139684-102139924 | Rare:84 | ||||
chr14:102362856-102363098 | Rare:106 | ||||
chr14:103385266-103385449 | Common:1; Rare:66 | ||||
chr14:103529035-103529258 | Common:1; Rare:69 | ||||
chr14:103562620-103563044 | Common:8; Rare:165; Clinvar (benign):5 | ||||
chr14:103715397-103715867 | Common:1; Rare:161 | ||||
chr14:105248431-105248628 | Common:5; Rare:96 | ||||
chr15:29822035-29822225 | Rare:64 | ||||
chr15:29822431-29822631 | Common:2; Rare:76 | ||||
chr15:32615397-32615528 | Common:3; Rare:34 | ||||
chr15:32717660-32718035 | Common:1; Rare:102 | ||||
chr15:34101843-34102080 | Common:1; Rare:47 | ||||
chr15:34367166-34367320 | Common:1; Rare:62 |