Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:186375186-186375548 | Rare:85 | ||||
chr1:186375672-186375945 | Common:1; Rare:72 | ||||
chr1:186680326-186680715 | Common:3; Rare:86 | ||||
chr1:186680765-186680902 | Rare:29 | ||||
chr1:192808746-192809061 | Common:4; Rare:119 | ||||
chr1:193059185-193059549 | Rare:138 | ||||
chr1:193059555-193059769 | Common:1; Rare:108 | ||||
chr1:193105275-193105696 | Common:4; Rare:176 | ||||
chr1:193121926-193122284 | Common:1; Rare:112; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
chr1:197146577-197146820 | Rare:58; Clinvar:3 | ||||
chr1:197902400-197902652 | Common:1; Rare:64 | ||||
chr1:197917307-197917389 | Rare:26 | ||||
chr1:198156851-198157067 | Common:5; Rare:84 | ||||
chr1:200409949-200410237 | Rare:93 | ||||
chr1:200669804-200670110 | Common:12; Rare:97 |