Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:37989944-37990167 | Rare:82 | ||||
chr1:38012537-38012799 | Rare:80 | ||||
chr1:38859712-38859984 | Rare:106 | ||||
chr1:38873306-38873540 | Common:3; Rare:81 | ||||
chr1:40040444-40040801 | Common:3; Rare:108 | ||||
chr1:40161265-40161402 | Rare:37 | ||||
chr1:40257908-40258282 | Common:4; Rare:101; Clinvar:7; Clinvar (benign):1 | ||||
chr1:40508626-40508822 | Common:6; Rare:61 | ||||
chr1:40531509-40531653 | Rare:32 | ||||
chr1:40691542-40691831 | Common:2; Rare:139 | ||||
chr1:40692062-40692132 | Rare:29 | ||||
chr1:40979636-40979755 | Common:1; Rare:40 | ||||
chr1:42335134-42335346 | Common:4; Rare:111 | ||||
chr1:42456004-42456370 | Common:1; Rare:99 | ||||
chr1:42456446-42456583 | Rare:59 |