Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:31457360-31457577 | Common:2; Rare:77 | ||||
chr14:31561328-31561491 | Common:2; Rare:63; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr14:32076026-32076308 | Common:2; Rare:72 | ||||
chr14:32076651-32077051 | Common:3; Rare:118 | ||||
chr14:34462214-34462551 | Common:1; Rare:116 | ||||
chr14:34539595-34539764 | Rare:63 | ||||
chr14:34714538-34714793 | Common:4; Rare:94 | ||||
chr14:34982373-34982682 | Common:1; Rare:121 | ||||
chr14:35046130-35046571 | Common:1; Rare:150 | ||||
chr14:35121920-35122605 | Common:3; Rare:202 | ||||
chr14:35292187-35292471 | Common:5; Rare:105; Clinvar:1 | ||||
chr14:35826244-35826487 | Common:1; Rare:71 | ||||
chr14:35826717-35826926 | Common:1; Rare:55 | ||||
chr14:36320572-36320796 | Common:3; Rare:71 | ||||
chr14:37197819-37198102 | Common:3; Rare:95 |