Proximal

BJ(Human) | 3906 records |

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Coordinate	Validation	Epigenomic status	Core promoter element(s)	Mutation	TF registry
chr7:87876324-87876614				Common:2; Rare:124
chr7:91880658-91880804				Common:1; Rare:41
chr7:92134442-92134567				Rare:37
chr7:92245835-92246274				Common:6; Rare:110; Clinvar:4; Clinvar (benign):5
chr7:92528528-92528831				Common:3; Rare:98; Clinvar (benign):1
chr7:94394532-94395084				Common:1; Rare:102; Clinvar:2; Clinvar (benign):3
chr7:94413892-94414275				Common:3; Rare:86; Clinvar:2; Clinvar (benign):3
chr7:94421901-94422184				Common:2; Rare:52; Clinvar (benign):1
chr7:94422490-94422779				Common:2; Rare:42
chr7:94423040-94423536				Common:5; Rare:100; Clinvar:2; Clinvar (pathogenic):1
chr7:94425040-94425225				Rare:54; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1
chr7:94425607-94425960				Rare:116; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1
chr7:94425993-94426299				Common:1; Rare:55; Clinvar:2; Clinvar (pathogenic):1
chr7:94656047-94656374				Common:2; Rare:91; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1
chr7:98252133-98252372				Common:1; Rare:54