Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:116667672-116667857 | Common:1; Rare:67 | ||||
chr1:117060037-117060359 | Common:7; Rare:86 | ||||
chr1:117929568-117929802 | Common:3; Rare:69 | ||||
chr1:119140632-119140776 | Common:1; Rare:48 | ||||
chr1:120176362-120176596 | Rare:53 | ||||
chr1:145823944-145824249 | Rare:109 | ||||
chr1:145859009-145859176 | Rare:44 | ||||
chr1:145859769-145859931 | Common:2; Rare:56 | ||||
chr1:145918695-145919013 | Common:2; Rare:64 | ||||
chr1:145927419-145927644 | Common:1; Rare:65; Clinvar (pathogenic):1 | ||||
chr1:145964590-145964742 | Rare:36 | ||||
chr1:145996555-145996882 | Common:1; Rare:125 | ||||
chr1:147172420-147172785 | Common:1; Rare:94 | ||||
chr1:147541246-147541583 | Common:1; Rare:54 | ||||
chr1:148458922-148459006 | Common:1; Rare:33 |