Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:151347195-151347487 | Rare:71 | ||||
chr1:151399494-151399602 | Common:1; Rare:40; Clinvar (pathogenic):1 | ||||
chr1:151427932-151428223 | Common:1; Rare:73; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:151511135-151511494 | Common:4; Rare:83 | ||||
chr1:151611846-151612313 | Common:4; Rare:117; Clinvar:1; Clinvar (benign):2 | ||||
chr1:151710280-151710458 | Rare:39 | ||||
chr1:151721277-151721560 | Common:2; Rare:75 | ||||
chr1:151760846-151761035 | Common:2; Rare:68 | ||||
chr1:151763451-151763672 | Common:2; Rare:88 | ||||
chr1:151766568-151766868 | Common:1; Rare:92 | ||||
chr1:151767137-151767173 | Rare:7 | ||||
chr1:151790415-151790871 | Common:3; Rare:110 | ||||
chr1:151831767-151831882 | Rare:30 | ||||
chr1:151909359-151909709 | Common:4; Rare:127 | ||||
chr1:151992566-151992746 | Common:1; Rare:37 |