Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:119759707-119759922 | Common:1; Rare:61 | ||||
chr2:119760046-119760270 | Common:1; Rare:49 | ||||
chr2:120223378-120223535 | Common:1; Rare:50 | ||||
chr2:120252591-120252964 | Common:3; Rare:122 | ||||
chr2:121285092-121285347 | Common:2; Rare:97 | ||||
chr2:121530552-121530889 | Common:8; Rare:141; Clinvar (pathogenic):1 | ||||
chr2:121649374-121649830 | Common:3; Rare:130 | ||||
chr2:121650011-121650157 | Rare:39 | ||||
chr2:121736736-121737242 | Common:5; Rare:203 | ||||
chr2:121755415-121755809 | Common:5; Rare:132 | ||||
chr2:126655188-126655455 | Common:1; Rare:63 | ||||
chr2:126655754-126656306 | Common:1; Rare:154; Clinvar:2 | ||||
chr2:127106944-127107264 | Common:1; Rare:96; Clinvar:8; Clinvar (benign):2 | ||||
chr2:127294077-127294205 | Common:2; Rare:48; Clinvar:1; Clinvar (benign):2 | ||||
chr2:127387231-127387450 | Common:4; Rare:75 |