Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:102362862-102363092 | Rare:103 | ||||
chr14:103333909-103334258 | Common:3; Rare:146 | ||||
chr14:103562624-103563028 | Common:7; Rare:151; Clinvar (benign):3 | ||||
chr14:104970428-104970840 | Common:5; Rare:78 | ||||
chr14:105021041-105021417 | Common:1; Rare:135 | ||||
chr15:22838481-22838723 | Common:2; Rare:98 | ||||
chr15:29269785-29269878 | Rare:37 | ||||
chr15:30903718-30903950 | Common:1; Rare:59 | ||||
chr15:32615122-32615566 | Common:6; Rare:114 | ||||
chr15:34101835-34102083 | Common:1; Rare:52 | ||||
chr15:34582835-34582942 | Rare:38 | ||||
chr15:35546137-35546263 | Common:1; Rare:44 | ||||
chr15:36579518-36579784 | Common:4; Rare:73 | ||||
chr15:37100344-37100784 | Common:1; Rare:135 | ||||
chr15:39580813-39581097 | Common:1; Rare:78 |