Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:2336420-2336546 | Rare:50 | ||||
chr17:2711755-2712012 | Common:1; Rare:76 | ||||
chr17:3636241-3636484 | Common:4; Rare:66; Clinvar (benign):1 | ||||
chr17:3636596-3636775 | Common:2; Rare:51; Clinvar:3; Clinvar (benign):2 | ||||
chr17:3668527-3668819 | Common:3; Rare:118 | ||||
chr17:3723795-3723925 | Common:1; Rare:70 | ||||
chr17:4142967-4143230 | Common:3; Rare:91 | ||||
chr17:4263948-4264064 | Rare:48 | ||||
chr17:4704092-4704245 | Rare:79 | ||||
chr17:4807007-4807185 | Common:3; Rare:60 | ||||
chr17:4939906-4940344 | Common:2; Rare:129 | ||||
chr17:4967754-4968261 | Common:3; Rare:161 | ||||
chr17:5419651-5419774 | Common:2; Rare:45 | ||||
chr17:5420054-5420202 | Rare:58 | ||||
chr17:5486313-5486573 | Common:4; Rare:68 |