Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:160262442-160262702 | Common:1; Rare:81 | ||||
chr1:160343184-160343386 | Rare:80 | ||||
chr1:161118022-161118105 | Rare:37 | ||||
chr1:161766234-161766360 | Common:3; Rare:41 | ||||
chr1:165768830-165768908 | Common:1; Rare:37 | ||||
chr1:174999657-175000095 | Common:1; Rare:123 | ||||
chr1:179143052-179143248 | Rare:38 | ||||
chr1:186375675-186375921 | Common:1; Rare:64 | ||||
chr1:193059306-193059665 | Rare:167 | ||||
chr1:193186568-193186677 | Rare:18 | ||||
chr1:201377621-201378066 | Common:4; Rare:98; Clinvar:1; Clinvar (benign):2 | ||||
chr1:201946505-201946788 | Common:2; Rare:46 | ||||
chr1:207751933-207752124 | Common:1; Rare:67 | ||||
chr1:212791766-212791933 | Common:3; Rare:67 | ||||
chr1:217631045-217631365 | Common:2; Rare:83 |