Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:200483565-200483748 | Rare:31 | ||||
chr1:200738741-200738961 | Common:6; Rare:69 | ||||
chr1:203627945-203628057 | Rare:17 | ||||
chr1:204190952-204191108 | Rare:20 | ||||
chr1:210233784-210233983 | Common:1; Rare:64 | ||||
chr1:220876643-220876812 | Rare:31 | ||||
chr1:222711484-222711649 | Rare:33 | ||||
chr1:223992564-223992812 | Common:4; Rare:89 | ||||
chr1:234721945-234722256 | Common:2; Rare:59 | ||||
chr1:234987398-234987685 | Common:4; Rare:40 | ||||
chr1:244451121-244451245 | Common:2; Rare:33 | ||||
chr1:244863676-244863788 | Rare:38; Clinvar:1; Clinvar (benign):2 | ||||
chr1:246569747-246569876 | Common:1; Rare:23 | ||||
chr1:246609043-246609305 | Common:1; Rare:47 | ||||
chr10:3783017-3783088 | Rare:20 |