Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:76867277-76867494 | Rare:46 | ||||
chr1:77219391-77219509 | Rare:54 | ||||
chr1:77888318-77888758 | Common:2; Rare:97; Clinvar:2; Clinvar (benign):1 | ||||
chr1:77955255-77955584 | Rare:68 | ||||
chr1:77979000-77979336 | Common:3; Rare:115 | ||||
chr1:77979468-77979553 | Common:1; Rare:25 | ||||
chr1:78004547-78005001 | Common:4; Rare:99 | ||||
chr1:78045863-78045937 | Rare:23 | ||||
chr1:78045942-78046334 | Common:1; Rare:147 | ||||
chr1:78046356-78046418 | Common:1; Rare:32 | ||||
chr1:81306246-81306348 | Rare:20 | ||||
chr1:81306354-81306423 | Rare:10 | ||||
chr1:84077864-84078197 | Common:1; Rare:119 | ||||
chr1:84298408-84298549 | Common:1; Rare:43 | ||||
chr1:84479208-84479334 | Common:3; Rare:66 |