Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:236523322-236523722 | Common:3; Rare:90 | ||||
chr1:236523726-236524077 | Common:19; Rare:344 | ||||
chr1:236524358-236524970 | Common:15; Rare:491 | ||||
chr1:236603918-236604318 | Common:2; Rare:130 | ||||
chr1:236604385-236604785 | Common:27; Rare:434 | ||||
chr1:236604792-236604970 | Rare:40 | ||||
chr1:236686150-236686570 | Common:1; Rare:304 | ||||
chr1:236794984-236795450 | Common:27; Rare:678; Clinvar:12 | ||||
chr1:236795726-236796483 | Common:5; Rare:337; Clinvar:1; Clinvar (benign):1 | ||||
chr1:239718971-239719371 | Common:3; Rare:99 | ||||
chr1:241518983-241519383 | Common:1; Rare:103 | ||||
chr1:241519607-241520059 | Common:15; Rare:746; Clinvar:80; Clinvar (benign):55; Clinvar (pathogenic):23 | ||||
chr1:241531257-241532006 | Common:7; Rare:275 | ||||
chr1:241639266-241640630 | Common:43; Rare:963 | ||||
chr1:241770130-241770550 | Common:7; Rare:102 |