Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:38012934-38013124 | Common:1; Rare:45 | ||||
chr1:38859712-38860025 | Rare:115 | ||||
chr1:38873306-38873563 | Common:3; Rare:91 | ||||
chr1:39026109-39026398 | Common:1; Rare:69 | ||||
chr1:39081179-39081506 | Common:3; Rare:67 | ||||
chr1:39268359-39268494 | Rare:23 | ||||
chr1:39691381-39691550 | Common:3; Rare:29 | ||||
chr1:39738710-39739059 | Common:3; Rare:87 | ||||
chr1:39883394-39883610 | Common:1; Rare:88; Clinvar (pathogenic):1 | ||||
chr1:40040444-40040806 | Common:3; Rare:110 | ||||
chr1:40097229-40097343 | Common:1; Rare:47; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
chr1:40161098-40161402 | Common:1; Rare:71 | ||||
chr1:40257862-40258310 | Common:4; Rare:121; Clinvar:8; Clinvar (benign):1 | ||||
chr1:40373513-40373795 | Common:1; Rare:67 | ||||
chr1:40374566-40374669 | Common:12; Rare:23 |