Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161132412-161132621 | Common:1; Rare:68 | ||||
chr1:161132625-161132648 | Rare:10 | ||||
chr1:161197210-161197457 | Common:3; Rare:45 | ||||
chr1:161209888-161210185 | Common:1; Rare:77; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr1:163321731-163322013 | Common:1; Rare:77 | ||||
chr1:165768799-165768947 | Common:2; Rare:70 | ||||
chr1:167935952-167936329 | Common:2; Rare:114 | ||||
chr1:167936559-167936705 | Rare:48 | ||||
chr1:168225712-168226026 | Common:2; Rare:101 | ||||
chr1:169367739-169367956 | Common:2; Rare:49 | ||||
chr1:169485930-169486159 | Rare:55; Clinvar:1 | ||||
chr1:169794890-169795052 | Common:3; Rare:34 | ||||
chr1:170664093-170664257 | Common:3; Rare:49 | ||||
chr1:171485373-171485569 | Rare:72 | ||||
chr1:171841358-171841546 | Common:3; Rare:58 |