Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:173509545-173509683 | Common:1; Rare:34 | ||||
chr4:176320519-176320617 | Rare:32 | ||||
chr4:184392976-184393222 | Common:2; Rare:47 | ||||
chr4:184537509-184537661 | Common:3; Rare:39 | ||||
chr4:184803078-184803378 | Common:1; Rare:68 | ||||
chr4:184813367-184813693 | Common:2; Rare:68 | ||||
chr4:184813803-184813832 | Rare:5 | ||||
chr4:184823156-184823358 | Rare:30 | ||||
chr4:184850567-184850611 | Rare:5 | ||||
chr4:184851088-184851192 | Rare:14 | ||||
chr4:184851230-184851268 | Rare:8 | ||||
chr4:184894229-184894484 | Common:1; Rare:63 | ||||
chr4:185504547-185504682 | Common:1; Rare:36; Clinvar:2; Clinvar (benign):1 | ||||
chr4:189787548-189787905 | Common:4; Rare:57 | ||||
chr5:784692-784904 | Common:5; Rare:70 |