Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:102139678-102139925 | Rare:85 | ||||
chr14:102305124-102305299 | Common:1; Rare:59 | ||||
chr14:102362858-102363075 | Rare:102 | ||||
chr14:103333924-103334256 | Common:3; Rare:141 | ||||
chr14:103529116-103529223 | Common:1; Rare:38 | ||||
chr14:103562624-103563053 | Common:8; Rare:170; Clinvar (benign):5 | ||||
chr14:104970465-104970606 | Common:3; Rare:23 | ||||
chr15:22838481-22838753 | Common:2; Rare:110 | ||||
chr15:30903614-30903929 | Common:3; Rare:84 | ||||
chr15:34101821-34102083 | Common:1; Rare:59 | ||||
chr15:34224952-34225070 | Rare:42 | ||||
chr15:35546142-35546215 | Rare:30 | ||||
chr15:37099651-37099744 | Rare:20 | ||||
chr15:37100488-37100783 | Common:1; Rare:100 | ||||
chr15:38253155-38253179 | Rare:12; Clinvar:2 |