Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:19155275-19155641 | Common:4; Rare:83 | ||||
chr9:23234003-23234094 | Rare:23 | ||||
chr9:32436055-32436389 | Common:2; Rare:97 | ||||
chr9:33165849-33166045 | Common:1; Rare:37 | ||||
chr9:34380812-34380930 | Common:1; Rare:45 | ||||
chr9:35604026-35604230 | Common:3; Rare:58 | ||||
chr9:35723951-35724227 | Rare:68 | ||||
chr9:35724571-35724939 | Rare:81 | ||||
chr9:37780812-37781107 | Common:1; Rare:76; Clinvar (benign):2 | ||||
chr9:38437573-38437761 | Common:3; Rare:36 | ||||
chr9:40991963-40992410 | Common:7; Rare:32 | ||||
chr9:43119714-43119845 | Common:1; Rare:30 | ||||
chr9:62897698-62897954 | Common:8; Rare:49 | ||||
chr9:63326791-63327012 | Common:1; Rare:15 | ||||
chr9:63334304-63334516 | Rare:19 |