Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:92040035-92040164 | Common:2; Rare:29; Clinvar (benign):1 | ||||
chr14:92121667-92121982 | Common:4; Rare:105 | ||||
chr14:93184856-93185001 | Rare:45 | ||||
chr14:94081202-94081370 | Common:3; Rare:50 | ||||
chr14:96363336-96363550 | Common:1; Rare:69 | ||||
chr14:96502268-96502431 | Rare:64 | ||||
chr14:100376294-100376495 | Common:3; Rare:67 | ||||
chr14:102139684-102139916 | Rare:81 | ||||
chr14:102362858-102363084 | Rare:103 | ||||
chr14:103562624-103562996 | Common:5; Rare:132; Clinvar (benign):1 | ||||
chr15:30903704-30903912 | Common:1; Rare:50 | ||||
chr15:34101843-34102083 | Common:1; Rare:48 | ||||
chr15:34795531-34795924 | Common:1; Rare:79; Clinvar:4; Clinvar (benign):1 | ||||
chr15:39580843-39581083 | Rare:66 | ||||
chr15:40039092-40039350 | Rare:101 |