Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:160262424-160262642 | Common:1; Rare:69 | ||||
chr1:160285110-160285289 | Common:3; Rare:55; Clinvar:1; Clinvar (benign):2 | ||||
chr1:160343187-160343391 | Rare:85 | ||||
chr1:160400364-160400615 | Common:1; Rare:62 | ||||
chr1:161045888-161046057 | Common:1; Rare:44 | ||||
chr1:161098278-161098391 | Common:1; Rare:17 | ||||
chr1:161118012-161118141 | Rare:64 | ||||
chr1:161132583-161132848 | Common:2; Rare:79 | ||||
chr1:161159404-161159507 | Common:1; Rare:26 | ||||
chr1:161166309-161166514 | Common:2; Rare:50; Clinvar:3; Clinvar (benign):1 | ||||
chr1:161314260-161314437 | Common:3; Rare:74; Clinvar:10; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr1:161749632-161749826 | Rare:64 | ||||
chr1:162497761-162497849 | Common:1; Rare:28 | ||||
chr1:162790441-162790789 | Common:4; Rare:92 | ||||
chr1:163321713-163322073 | Common:1; Rare:95 |