Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:49598676-49599018 | Common:2; Rare:134 | ||||
chr14:49620573-49620817 | Common:2; Rare:96; Clinvar:1 | ||||
chr14:49688175-49688260 | Rare:35 | ||||
chr14:50312211-50312374 | Rare:62 | ||||
chr14:50944359-50944583 | Common:4; Rare:82; Clinvar:1; Clinvar (benign):2 | ||||
chr14:51240146-51240316 | Rare:80 | ||||
chr14:51651656-51651996 | Common:4; Rare:100 | ||||
chr14:52069007-52069358 | Common:2; Rare:73 | ||||
chr14:52314123-52314369 | Common:1; Rare:68 | ||||
chr14:52552516-52552855 | Common:1; Rare:94 | ||||
chr14:52707063-52707220 | Common:1; Rare:70 | ||||
chr14:52791423-52791821 | Common:2; Rare:127 | ||||
chr14:52951010-52951342 | Common:4; Rare:123 | ||||
chr14:53152379-53152450 | Rare:27 | ||||
chr14:54441249-54441489 | Rare:96 |