Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:32963797-32964197 | Rare:96 | ||||
chr1:32964229-32964304 | Rare:18 | ||||
chr1:32964312-32964512 | Common:2; Rare:55 | ||||
chr1:32964519-32964647 | Rare:32 | ||||
chr1:32964653-32965060 | Common:2; Rare:147 | ||||
chr1:33036170-33036360 | Rare:28 | ||||
chr1:33036766-33037201 | Common:1; Rare:157; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr1:33080925-33081218 | Common:3; Rare:84 | ||||
chr1:33182000-33182247 | Rare:53 | ||||
chr1:33256097-33256653 | Common:1; Rare:141 | ||||
chr1:33256805-33257066 | Common:4; Rare:74 | ||||
chr1:33257076-33257111 | Rare:8 | ||||
chr1:33349194-33349287 | Common:2; Rare:23 | ||||
chr1:33349452-33349575 | Rare:30 | ||||
chr1:33349702-33350324 | Common:3; Rare:193 |