Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:206084613-206084667 | Rare:10 | ||||
chr2:207163487-207163746 | Common:1; Rare:41 | ||||
chr2:215397678-215397974 | Common:1; Rare:80 | ||||
chr2:215433550-215433833 | Common:1; Rare:59 | ||||
chr2:217829844-217829990 | Common:2; Rare:41 | ||||
chr2:217920900-217921086 | Common:3; Rare:34 | ||||
chr2:217929896-217930132 | Common:1; Rare:40 | ||||
chr2:217957268-217957394 | Common:4; Rare:17 | ||||
chr2:217966031-217966228 | Rare:38 | ||||
chr2:217979957-217980160 | Rare:37 | ||||
chr2:218272487-218272630 | Common:1; Rare:49 | ||||
chr2:218277059-218277303 | Common:2; Rare:47 | ||||
chr2:218402615-218402714 | Rare:37 | ||||
chr2:237324588-237325048 | Common:3; Rare:117; Clinvar:3; Clinvar (benign):6 | ||||
chr2:238727583-238727825 | Common:2; Rare:39 |