Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:156752393-156752512 | Rare:32 | ||||
chr1:156767372-156767574 | Common:1; Rare:69 | ||||
chr1:156859068-156859143 | Common:2; Rare:24 | ||||
chr1:156860673-156860956 | Common:3; Rare:80; Clinvar:2; Clinvar (benign):4 | ||||
chr1:157138342-157138710 | Common:5; Rare:116 | ||||
chr1:159005685-159005981 | Common:4; Rare:53 | ||||
chr1:159171400-159171617 | Rare:61 | ||||
chr1:159925456-159925617 | Common:1; Rare:42 | ||||
chr1:159945592-159945815 | Common:2; Rare:56 | ||||
chr1:160031809-160032060 | Common:2; Rare:67 | ||||
chr1:160081402-160081570 | Rare:35 | ||||
chr1:160205241-160205453 | Common:2; Rare:61 | ||||
chr1:160262115-160262293 | Rare:49 | ||||
chr1:160262415-160262664 | Common:1; Rare:77 | ||||
chr1:160285092-160285236 | Common:3; Rare:55; Clinvar:2; Clinvar (benign):4 |