Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:99141128-99141776 | Common:3; Rare:233 | ||||
chr2:99154883-99155079 | Common:2; Rare:76; Clinvar (benign):3 | ||||
chr2:99180947-99181226 | Common:2; Rare:89 | ||||
chr2:100417374-100417679 | Rare:91 | ||||
chr2:100562715-100563054 | Common:3; Rare:108 | ||||
chr2:101002162-101002325 | Rare:63 | ||||
chr2:102736817-102736951 | Common:1; Rare:69 | ||||
chr2:105037718-105038165 | Common:5; Rare:143 | ||||
chr2:105337473-105337606 | Common:1; Rare:64 | ||||
chr2:105398955-105399235 | Common:1; Rare:101 | ||||
chr2:106194210-106194573 | Common:6; Rare:155 | ||||
chr2:108288879-108289049 | Common:1; Rare:27 | ||||
chr2:108449104-108449271 | Rare:64 | ||||
chr2:108534133-108534551 | Common:8; Rare:165 | ||||
chr2:108588164-108588379 | Common:2; Rare:40 |