Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161750220-161750436 | Rare:52 | ||||
chr1:162023351-162023482 | Common:1; Rare:42; Clinvar (pathogenic):1 | ||||
chr1:162023625-162023981 | Common:1; Rare:101 | ||||
chr1:162561351-162561730 | Common:4; Rare:146 | ||||
chr1:162631108-162631377 | Common:5; Rare:54 | ||||
chr1:162631616-162632022 | Rare:78 | ||||
chr1:162632256-162632563 | Rare:60 | ||||
chr1:162790516-162790797 | Common:4; Rare:84 | ||||
chr1:163202797-163203040 | Rare:47 | ||||
chr1:163203052-163203246 | Common:1; Rare:38 | ||||
chr1:163321713-163322057 | Common:1; Rare:94 | ||||
chr1:164558794-164559184 | Common:1; Rare:108 | ||||
chr1:165698377-165698708 | Common:3; Rare:143 | ||||
chr1:165768650-165768955 | Common:2; Rare:117; Clinvar:1 | ||||
chr1:165827755-165827829 | Rare:21 |