Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:85612018-85612104 | Rare:27 | ||||
chr2:85888906-85889113 | Common:2; Rare:70; Clinvar:2; Clinvar (benign):2 | ||||
chr2:86105797-86106250 | Common:2; Rare:134 | ||||
chr2:86441152-86441382 | Common:1; Rare:77 | ||||
chr2:88627412-88627733 | Common:3; Rare:81; Clinvar:4; Clinvar (benign):1 | ||||
chr2:95165651-95165825 | Rare:52 | ||||
chr2:95402618-95402747 | Rare:43 | ||||
chr2:96208252-96208407 | Rare:79 | ||||
chr2:96208781-96208942 | Common:3; Rare:64 | ||||
chr2:96265947-96266306 | Common:2; Rare:104; Clinvar:2 | ||||
chr2:97645938-97646095 | Common:1; Rare:56 | ||||
chr2:97663993-97664245 | Rare:75 | ||||
chr2:98608447-98608665 | Common:1; Rare:95 | ||||
chr2:99154886-99155036 | Common:1; Rare:63 | ||||
chr2:99180979-99181249 | Common:2; Rare:78 |