Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:6473092-6473428 | Common:2; Rare:123; Clinvar:15; Clinvar (benign):9 | ||||
chr1:7128681-7128821 | Rare:25 | ||||
chr1:7704562-7704869 | Common:4; Rare:133 | ||||
chr1:7812656-7812773 | Rare:20 | ||||
chr1:7973934-7973997 | Rare:15 | ||||
chr1:8024621-8024841 | Rare:32 | ||||
chr1:8369371-8369499 | Rare:20 | ||||
chr1:9162931-9163207 | Common:2; Rare:44 | ||||
chr1:9182094-9182247 | Common:1; Rare:42 | ||||
chr1:9182276-9182314 | Rare:8 | ||||
chr1:9191727-9191814 | Common:1; Rare:19 | ||||
chr1:9356429-9356745 | Common:2; Rare:61 | ||||
chr1:9739495-9739809 | Common:2; Rare:54 | ||||
chr1:9909281-9909426 | Rare:24 | ||||
chr1:10296587-10296919 | Common:1; Rare:79; Clinvar:1; Clinvar (benign):1 |