Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:102362858-102363069 | Rare:99 | ||||
chr14:103562624-103563043 | Common:8; Rare:163; Clinvar (benign):5 | ||||
chr15:34101843-34102060 | Rare:44 | ||||
chr15:35546166-35546252 | Common:1; Rare:30 | ||||
chr15:39920137-39920356 | Common:1; Rare:38 | ||||
chr15:40039112-40039350 | Rare:96 | ||||
chr15:40755220-40755432 | Common:2; Rare:69 | ||||
chr15:40807430-40807761 | Common:4; Rare:109 | ||||
chr15:42208284-42208404 | Rare:37 | ||||
chr15:42273400-42273619 | Rare:79 | ||||
chr15:42548774-42548879 | Common:1; Rare:62 | ||||
chr15:43826905-43827039 | Rare:57 | ||||
chr15:44536865-44537079 | Common:1; Rare:61 | ||||
chr15:44711292-44711577 | Rare:78; Clinvar:1 | ||||
chr15:45023052-45023233 | Common:3; Rare:47 |