Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:50545681-50545918 | Common:1; Rare:42 | ||||
chr3:4751612-4751824 | Common:3; Rare:43 | ||||
chr3:4831347-4831599 | Common:3; Rare:47 | ||||
chr3:8444410-8444642 | Common:3; Rare:43 | ||||
chr3:9396285-9396325 | Rare:21 | ||||
chr3:14945788-14946033 | Rare:66 | ||||
chr3:15037813-15038114 | Common:1; Rare:64 | ||||
chr3:48578327-48578397 | Rare:18; Clinvar (pathogenic):1 | ||||
chr3:75435017-75435385 | Common:5; Rare:125 | ||||
chr3:75641103-75641403 | Common:1; Rare:47 | ||||
chr3:75672465-75672745 | Rare:1 | ||||
chr3:98980996-98981092 | Rare:19 | ||||
chr3:98981116-98981375 | Common:2; Rare:37 | ||||
chr3:98986164-98986407 | Rare:45 | ||||
chr3:101576978-101577041 | Common:1; Rare:14 |