Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:95788788-95789188 | Common:1; Rare:158 | ||||
chr11:95789460-95790201 | Common:27; Rare:992 | ||||
chr11:95790162-95790737 | Common:10; Rare:840; Clinvar:2 | ||||
chr11:95790900-95791460 | Common:5; Rare:423 | ||||
chr11:95923043-95923443 | Common:4; Rare:66 | ||||
chr11:95923758-95924540 | Common:9; Rare:968; Clinvar:22; Clinvar (benign):23 | ||||
chr11:95924592-95924875 | Common:2; Rare:55 | ||||
chr11:96342130-96343413 | Common:12; Rare:473 | ||||
chr11:96388607-96389007 | Common:1; Rare:62 | ||||
chr11:96389170-96389530 | Common:3; Rare:103 | ||||
chr11:96389680-96390150 | Common:11; Rare:763 | ||||
chr11:96390325-96390725 | Common:1; Rare:80 | ||||
chr11:99020320-99021063 | Common:5; Rare:514 | ||||
chr11:100686870-100687932 | Common:18; Rare:646 | ||||
chr11:100687860-100688140 | Common:2; Rare:78 |