Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr12:123233093-123233490 | Common:2; Rare:132; Clinvar:1 | ||||
chr12:123364812-123364932 | Common:1; Rare:47 | ||||
chr12:123533289-123533321 | Common:1; Rare:9 | ||||
chr12:123584317-123584669 | Common:8; Rare:125 | ||||
chr12:123601829-123602174 | Common:6; Rare:98 | ||||
chr12:123633633-123633845 | Common:1; Rare:96; Clinvar:8; Clinvar (benign):1 | ||||
chr12:123972551-123972905 | Common:6; Rare:120 | ||||
chr12:123972985-123973299 | Common:2; Rare:95 | ||||
chr12:124388785-124388978 | Common:3; Rare:63 | ||||
chr12:124430732-124430968 | Common:1; Rare:86 | ||||
chr12:125065319-125065479 | Common:1; Rare:61 | ||||
chr12:128824011-128824100 | Common:1; Rare:29 | ||||
chr12:130839125-130839382 | Common:2; Rare:91 | ||||
chr12:130871730-130872110 | Common:4; Rare:159 | ||||
chr12:131710825-131711125 | Rare:75 |