Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:43367986-43368252 | Rare:73 | ||||
chr1:43389777-43389937 | Common:3; Rare:61 | ||||
chr1:43649882-43650197 | Rare:77 | ||||
chr1:43707366-43707566 | Common:2; Rare:53 | ||||
chr1:43974812-43974991 | Common:3; Rare:53 | ||||
chr1:44674457-44674758 | Common:2; Rare:69 | ||||
chr1:44775848-44776138 | Common:2; Rare:107 | ||||
chr1:45500002-45500335 | Common:2; Rare:75; Clinvar:4; Clinvar (pathogenic):2 | ||||
chr1:45583931-45584047 | Rare:42 | ||||
chr1:45688049-45688211 | Common:1; Rare:39 | ||||
chr1:45750602-45750842 | Rare:85 | ||||
chr1:46303596-46303715 | Common:1; Rare:30 | ||||
chr1:50970121-50970287 | Common:1; Rare:27 | ||||
chr1:52055192-52055259 | Rare:17 | ||||
chr1:52056085-52056335 | Common:2; Rare:73 |