Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:86756238-86756616 | Common:4; Rare:130 | ||||
chr10:86957522-86957749 | Rare:57 | ||||
chr10:86958459-86958676 | Rare:58 | ||||
chr10:86959145-86959450 | Common:3; Rare:59 | ||||
chr10:86968181-86968556 | Common:5; Rare:86 | ||||
chr10:86969923-86969985 | Rare:10 | ||||
chr10:87094891-87095235 | Common:1; Rare:83; Clinvar:2 | ||||
chr10:87504801-87504952 | Common:1; Rare:77 | ||||
chr10:87818150-87818324 | Rare:65 | ||||
chr10:87863996-87864527 | Common:2; Rare:153; Clinvar:17; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
chr10:88583196-88583463 | Rare:82 | ||||
chr10:88880382-88880529 | Rare:22 | ||||
chr10:88952716-88953061 | Common:2; Rare:59; Clinvar:1 | ||||
chr10:88990469-88990882 | Common:5; Rare:113; Clinvar:1; Clinvar (benign):5 | ||||
chr10:88991285-88991451 | Common:2; Rare:34 |