Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:17439669-17439883 | Rare:69 | ||||
chr1:19210071-19210401 | Rare:116 | ||||
chr1:19251480-19251866 | Common:6; Rare:133 | ||||
chr1:19311997-19312350 | Common:8; Rare:166 | ||||
chr1:19485446-19485765 | Rare:120 | ||||
chr1:20486198-20486363 | Rare:36 | ||||
chr1:20508038-20508181 | Common:2; Rare:54 | ||||
chr1:20661340-20661730 | Common:3; Rare:140; Clinvar:4; Clinvar (benign):6 | ||||
chr1:20787230-20787414 | Rare:95 | ||||
chr1:21176836-21177092 | Rare:73 | ||||
chr1:21345454-21345655 | Common:2; Rare:75 | ||||
chr1:21783083-21783288 | Common:2; Rare:74 | ||||
chr1:23019294-23019503 | Rare:62 | ||||
chr1:23344233-23344576 | Common:2; Rare:112 | ||||
chr1:23368305-23368502 | Common:1; Rare:49 |