Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:1324586-1324835 | Common:3; Rare:134 | ||||
chr1:1399315-1399589 | Common:1; Rare:122 | ||||
chr1:1724319-1724471 | Common:3; Rare:54 | ||||
chr1:2391540-2391868 | Common:2; Rare:120 | ||||
chr1:3900228-3900352 | Common:10; Rare:60 | ||||
chr1:8878624-8878874 | Rare:136 | ||||
chr1:9943339-9943488 | Common:2; Rare:34 | ||||
chr1:15526551-15526885 | Common:2; Rare:103 | ||||
chr1:19251512-19251830 | Common:6; Rare:102 | ||||
chr1:20508117-20508202 | Rare:23 | ||||
chr1:23559427-23559648 | Common:1; Rare:94 | ||||
chr1:25232468-25232582 | Rare:40 | ||||
chr1:25859370-25859578 | Common:2; Rare:84 | ||||
chr1:26432111-26432356 | Common:4; Rare:70; Clinvar:2; Clinvar (benign):1 | ||||
chr1:28505823-28506045 | Common:2; Rare:85 |