Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:96502316-96502601 | Common:1; Rare:125 | ||||
chr14:100019281-100019497 | Common:2; Rare:40 | ||||
chr14:100306424-100306735 | Common:3; Rare:112 | ||||
chr14:100375324-100375758 | Common:4; Rare:73 | ||||
chr14:100376259-100376514 | Common:3; Rare:81 | ||||
chr14:102139684-102139943 | Rare:90 | ||||
chr14:102235386-102235748 | Rare:80 | ||||
chr14:102362856-102363098 | Rare:106 | ||||
chr14:102592368-102592675 | Common:1; Rare:129 | ||||
chr14:103333929-103334263 | Common:3; Rare:140 | ||||
chr14:103335855-103336066 | Rare:78 | ||||
chr14:103529019-103529260 | Common:1; Rare:73 | ||||
chr14:103562620-103563275 | Common:11; Rare:268; Clinvar:1; Clinvar (benign):9 | ||||
chr14:103629377-103629490 | Common:2; Rare:40 | ||||
chr14:103715419-103715853 | Common:1; Rare:148 |