Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:2701194-2701471 | Rare:102 | ||||
chr17:2711762-2712031 | Common:2; Rare:75 | ||||
chr17:3636241-3636505 | Common:4; Rare:74; Clinvar (benign):1 | ||||
chr17:3636648-3636772 | Common:1; Rare:29; Clinvar:2; Clinvar (benign):1 | ||||
chr17:3668504-3668829 | Common:3; Rare:132 | ||||
chr17:3723749-3723917 | Common:1; Rare:92 | ||||
chr17:3845913-3846042 | Rare:34 | ||||
chr17:3892952-3893273 | Common:3; Rare:109 | ||||
chr17:4142954-4143244 | Common:3; Rare:101 | ||||
chr17:4143597-4143752 | Common:4; Rare:92 | ||||
chr17:4263943-4264042 | Rare:43 | ||||
chr17:4366628-4366795 | Common:1; Rare:68 | ||||
chr17:4555326-4555514 | Common:3; Rare:86 | ||||
chr17:4704088-4704250 | Rare:85 | ||||
chr17:4736337-4736373 | Rare:7 |