Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:75668860-75668891 | Common:1; Rare:3 | ||||
chr2:84970342-84970498 | Rare:47 | ||||
chr2:84991175-84991289 | Common:2; Rare:15 | ||||
chr2:85344085-85344242 | Common:4; Rare:73 | ||||
chr2:85421993-85422109 | Rare:10 | ||||
chr2:85540442-85540778 | Common:3; Rare:88 | ||||
chr2:85542527-85543087 | Common:3; Rare:150; Clinvar:1; Clinvar (benign):12 | ||||
chr2:85772416-85772635 | Rare:49 | ||||
chr2:85886567-85886844 | Common:2; Rare:49 | ||||
chr2:86135672-86135879 | Rare:52 | ||||
chr2:86136865-86137145 | Common:1; Rare:63 | ||||
chr2:86153559-86153756 | Rare:35 | ||||
chr2:86155536-86155579 | Rare:9 | ||||
chr2:86166602-86166704 | Rare:28 | ||||
chr2:86495922-86496008 | Rare:11 |