Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:31457360-31457554 | Common:2; Rare:72 | ||||
chr14:31561322-31561450 | Common:2; Rare:52; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr14:32076230-32076330 | Rare:28 | ||||
chr14:32076548-32077045 | Common:3; Rare:137 | ||||
chr14:32329183-32329408 | Rare:35 | ||||
chr14:34462203-34462602 | Common:1; Rare:138 | ||||
chr14:34539564-34539812 | Rare:87 | ||||
chr14:34629932-34630256 | Common:5; Rare:129 | ||||
chr14:34714538-34714754 | Common:3; Rare:80 | ||||
chr14:34982372-34982682 | Common:1; Rare:121 | ||||
chr14:35046139-35046636 | Common:1; Rare:170 | ||||
chr14:35121932-35122375 | Common:2; Rare:123 | ||||
chr14:35122497-35122699 | Common:2; Rare:60 | ||||
chr14:35292179-35292549 | Common:5; Rare:114; Clinvar:1 | ||||
chr14:35533930-35534164 | Common:3; Rare:92 |