Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:177392669-177392847 | Rare:63; Clinvar:1; Clinvar (benign):2 | ||||
chr2:178451095-178451365 | Common:5; Rare:79; Clinvar:3; Clinvar (benign):3 | ||||
chr2:181891669-181891981 | Common:4; Rare:125 | ||||
chr2:183124332-183124418 | Rare:33 | ||||
chr2:186486118-186486344 | Common:3; Rare:73 | ||||
chr2:189784294-189784518 | Common:4; Rare:75; Clinvar:7; Clinvar (benign):2 | ||||
chr2:191677858-191678143 | Common:4; Rare:80 | ||||
chr2:197453246-197453549 | Rare:100 | ||||
chr2:197499815-197500418 | Common:1; Rare:233; Clinvar:1; Clinvar (benign):1 | ||||
chr2:200811366-200811588 | Common:1; Rare:73 | ||||
chr2:200889035-200889391 | Common:2; Rare:116 | ||||
chr2:201071626-201072041 | Rare:86 | ||||
chr2:201451450-201451838 | Common:2; Rare:99 | ||||
chr2:201642637-201642722 | Rare:43 | ||||
chr2:203239000-203239026 | Rare:12 |