Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:149927748-149927917 | Common:1; Rare:65; Clinvar (benign):5 | ||||
chr1:150067665-150067893 | Rare:65 | ||||
chr1:150235950-150236389 | Common:1; Rare:101 | ||||
chr1:150272669-150272796 | Common:1; Rare:33 | ||||
chr1:150282279-150282596 | Common:3; Rare:66 | ||||
chr1:150293803-150293920 | Common:1; Rare:42 | ||||
chr1:150321421-150321599 | Rare:56; Clinvar:3; Clinvar (benign):1 | ||||
chr1:150363941-150364201 | Common:3; Rare:92 | ||||
chr1:150364579-150364730 | Common:1; Rare:50 | ||||
chr1:150487226-150487444 | Common:4; Rare:49; Clinvar (benign):3 | ||||
chr1:150578390-150578756 | Common:2; Rare:107 | ||||
chr1:150578922-150579005 | Common:1; Rare:34 | ||||
chr1:150579126-150579271 | Rare:62 | ||||
chr1:150579580-150579907 | Common:10; Rare:101 | ||||
chr1:150629462-150629858 | Common:1; Rare:91 |