Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:16155995-16156201 | Rare:47; Clinvar:2 | ||||
chr1:16206491-16206795 | Common:7; Rare:78 | ||||
chr1:16212516-16212763 | Common:1; Rare:46 | ||||
chr1:16352417-16352615 | Common:3; Rare:104 | ||||
chr1:16366967-16367299 | Common:1; Rare:104 | ||||
chr1:16921585-16921957 | Common:2; Rare:53 | ||||
chr1:17011855-17012114 | Common:1; Rare:76; Clinvar:2 | ||||
chr1:17053947-17054321 | Common:3; Rare:120; Clinvar:16; Clinvar (benign):12 | ||||
chr1:17248923-17249104 | Rare:39 | ||||
chr1:17438526-17438747 | Common:1; Rare:86 | ||||
chr1:17439501-17439853 | Rare:94 | ||||
chr1:17539558-17539756 | Rare:44 | ||||
chr1:18107362-18107532 | Rare:33 | ||||
chr1:18107536-18107839 | Common:4; Rare:58 | ||||
chr1:18480815-18481024 | Common:2; Rare:43 |