Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:151254627-151254785 | Rare:40 | ||||
chr1:151281963-151282318 | Rare:100 | ||||
chr1:151346843-151346970 | Rare:34 | ||||
chr1:151399419-151399587 | Common:1; Rare:51; Clinvar (pathogenic):1 | ||||
chr1:151540114-151540326 | Rare:56 | ||||
chr1:151763451-151763553 | Common:1; Rare:37 | ||||
chr1:151790473-151790849 | Common:2; Rare:82 | ||||
chr1:153535951-153536153 | Common:1; Rare:46 | ||||
chr1:153545595-153545863 | Rare:42 | ||||
chr1:153627498-153627880 | Common:2; Rare:82 | ||||
chr1:153628246-153628452 | Common:1; Rare:47 | ||||
chr1:153678581-153678655 | Rare:17 | ||||
chr1:153727739-153728078 | Common:1; Rare:105 | ||||
chr1:153963488-153963692 | Common:2; Rare:53 | ||||
chr1:153967306-153967512 | Common:1; Rare:42 |