Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:101308680-101308785 | Rare:41 | ||||
chr2:102064327-102064562 | Common:1; Rare:42 | ||||
chr2:102104363-102104699 | Common:6; Rare:76 | ||||
chr2:102141703-102141819 | Rare:19 | ||||
chr2:102142593-102142960 | Common:5; Rare:104 | ||||
chr2:102736846-102736928 | Common:1; Rare:34 | ||||
chr2:105037884-105038128 | Common:3; Rare:88 | ||||
chr2:105337463-105337618 | Common:1; Rare:72 | ||||
chr2:106194210-106194568 | Common:6; Rare:154 | ||||
chr2:108448903-108449257 | Common:1; Rare:114 | ||||
chr2:108534209-108534502 | Common:7; Rare:122 | ||||
chr2:108719383-108719654 | Common:3; Rare:114; Clinvar (benign):2 | ||||
chr2:109613808-109614024 | Common:2; Rare:74 | ||||
chr2:111884165-111884255 | Rare:23 | ||||
chr2:111898250-111898686 | Common:2; Rare:111 |