Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:98608313-98608806 | Common:2; Rare:185; Clinvar:1; Clinvar (benign):1 | ||||
chr2:99141141-99141794 | Common:3; Rare:229 | ||||
chr2:99154855-99155101 | Common:3; Rare:103; Clinvar (benign):3 | ||||
chr2:99180979-99181249 | Common:2; Rare:78 | ||||
chr2:99337239-99337585 | Rare:122 | ||||
chr2:99489904-99490308 | Common:1; Rare:168 | ||||
chr2:100322204-100322326 | Rare:30 | ||||
chr2:100322444-100322519 | Common:2; Rare:15 | ||||
chr2:100322521-100322620 | Common:1; Rare:30 | ||||
chr2:100417261-100417722 | Common:1; Rare:132 | ||||
chr2:100562732-100562828 | Rare:26 | ||||
chr2:100562847-100563059 | Common:3; Rare:71 | ||||
chr2:100563180-100563273 | Rare:31 | ||||
chr2:101002124-101002606 | Rare:154 | ||||
chr2:101252812-101252907 | Common:1; Rare:29 |