Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:18039089-18039486 | Common:5; Rare:105; Clinvar:1; Clinvar (benign):1 | ||||
chr17:18039542-18039703 | Rare:55 | ||||
chr17:18087758-18088011 | Rare:70 | ||||
chr17:18088299-18088308 | Rare:2 | ||||
chr17:18158153-18158308 | Common:1; Rare:36 | ||||
chr17:18182834-18183561 | Common:2; Rare:200 | ||||
chr17:18183678-18183977 | Rare:142 | ||||
chr17:18225355-18225655 | Common:3; Rare:94 | ||||
chr17:18257712-18258090 | Common:2; Rare:72 | ||||
chr17:18258157-18258237 | Rare:22 | ||||
chr17:18258537-18258647 | Common:2; Rare:32 | ||||
chr17:18258671-18258990 | Common:1; Rare:77 | ||||
chr17:18260451-18260701 | Rare:78 | ||||
chr17:18260805-18261021 | Common:2; Rare:52 | ||||
chr17:18314701-18314794 | Rare:32 |