Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:66354509-66354666 | Common:2; Rare:25 | ||||
chr1:66354787-66354870 | Rare:16 | ||||
chr1:66924820-66925074 | Rare:102 | ||||
chr1:66925207-66925525 | Common:2; Rare:99 | ||||
chr1:66930086-66930394 | Rare:99 | ||||
chr1:67054120-67054426 | Common:5; Rare:59 | ||||
chr1:67429989-67430279 | Rare:98 | ||||
chr1:67430292-67430544 | Rare:99 | ||||
chr1:67833342-67833524 | Common:2; Rare:72 | ||||
chr1:68232414-68232635 | Common:1; Rare:49 | ||||
chr1:68497006-68497153 | Common:1; Rare:53 | ||||
chr1:70205533-70205769 | Rare:78 | ||||
chr1:70221281-70221644 | Rare:141 | ||||
chr1:70354659-70354862 | Rare:67 | ||||
chr1:70411069-70411285 | Common:2; Rare:55; Clinvar:1; Clinvar (benign):1 |