Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:26279948-26280204 | Rare:140 | ||||
chr1:26432085-26432492 | Common:5; Rare:103; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26472274-26472618 | Common:4; Rare:127 | ||||
chr1:26472875-26473607 | Common:2; Rare:298 | ||||
chr1:26695444-26695786 | Rare:102 | ||||
chr1:26695942-26696103 | Rare:51 | ||||
chr1:26696866-26696921 | Rare:28; Clinvar:1; Clinvar (benign):1 | ||||
chr1:26787020-26787054 | Rare:7 | ||||
chr1:26787642-26788271 | Common:3; Rare:187; Clinvar:2; Clinvar (benign):2 | ||||
chr1:26826525-26826755 | Rare:77 | ||||
chr1:26890214-26890359 | Common:1; Rare:54 | ||||
chr1:26900035-26900209 | Rare:67 | ||||
chr1:26900390-26900554 | Rare:67 | ||||
chr1:26921543-26921874 | Common:3; Rare:105 | ||||
chr1:26945460-26945689 | Rare:62 |