Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:26764217-26764325 | Rare:42 | ||||
chr2:27212266-27212377 | Common:1; Rare:55 | ||||
chr2:27323043-27323136 | Rare:22; Clinvar (benign):1 | ||||
chr2:27356751-27357077 | Rare:93 | ||||
chr2:27370317-27370634 | Common:1; Rare:124 | ||||
chr2:27628981-27629069 | Common:1; Rare:43 | ||||
chr2:27663395-27663490 | Rare:19 | ||||
chr2:27663585-27663911 | Rare:115 | ||||
chr2:27771659-27771775 | Common:1; Rare:44 | ||||
chr2:27890615-27890825 | Rare:59 | ||||
chr2:28870262-28870463 | Rare:80 | ||||
chr2:32039743-32039848 | Rare:33 | ||||
chr2:37084346-37084551 | Common:3; Rare:78 | ||||
chr2:37156918-37157216 | Common:5; Rare:95 | ||||
chr2:37231559-37231702 | Common:4; Rare:78; Clinvar (benign):3 |