Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:176207226-176207344 | Common:1; Rare:61 | ||||
chr1:178725114-178725335 | Common:10; Rare:81 | ||||
chr1:178869150-178869363 | Common:1; Rare:38 | ||||
chr1:178870995-178871296 | Rare:59 | ||||
chr1:179081962-179082121 | Common:1; Rare:51 | ||||
chr1:179877766-179877982 | Rare:42 | ||||
chr1:179882176-179882361 | Rare:37 | ||||
chr1:179882488-179882841 | Rare:168; Clinvar:7; Clinvar (benign):2 | ||||
chr1:179954700-179954834 | Rare:28 | ||||
chr1:180154731-180155033 | Common:4; Rare:116 | ||||
chr1:180502502-180502922 | Common:2; Rare:164 | ||||
chr1:180912558-180912878 | Common:1; Rare:78 | ||||
chr1:181088537-181088704 | Rare:59 | ||||
chr1:182391273-182391489 | Rare:49 | ||||
chr1:182391679-182392045 | Common:5; Rare:132; Clinvar:5; Clinvar (benign):5 |