Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:85542520-85543085 | Common:3; Rare:152; Clinvar:1; Clinvar (benign):12 | ||||
chr2:87824888-87825102 | Rare:35 | ||||
chr2:87825118-87825296 | Common:3; Rare:42 | ||||
chr2:88016534-88016802 | Common:9; Rare:118 | ||||
chr2:88538425-88538712 | Rare:79 | ||||
chr2:88765732-88765916 | Rare:51 | ||||
chr2:96010451-96010552 | Rare:28 | ||||
chr2:96801070-96801342 | Rare:49 | ||||
chr2:96873041-96873292 | Common:3; Rare:49 | ||||
chr2:98597645-98597894 | Rare:56 | ||||
chr2:98614032-98614108 | Rare:8 | ||||
chr2:99123653-99123750 | Common:1; Rare:21 | ||||
chr2:99317497-99317509 | Rare:2 | ||||
chr2:99360235-99360546 | Common:1; Rare:74 | ||||
chr2:99390272-99390665 | Common:3; Rare:107 |