Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:4555317-4555515 | Common:3; Rare:92 | ||||
chr17:4704116-4704203 | Rare:55 | ||||
chr17:4710615-4710709 | Rare:32 | ||||
chr17:4807008-4807192 | Common:4; Rare:62 | ||||
chr17:4899384-4899456 | Common:1; Rare:48; Clinvar:1; Clinvar (benign):2 | ||||
chr17:4939916-4940341 | Common:2; Rare:126 | ||||
chr17:4948945-4949177 | Common:2; Rare:82 | ||||
chr17:4967733-4967963 | Rare:95 | ||||
chr17:4987424-4987765 | Common:3; Rare:109 | ||||
chr17:5078407-5078526 | Common:4; Rare:35 | ||||
chr17:5191838-5192077 | Common:1; Rare:79 | ||||
chr17:5419618-5419863 | Common:3; Rare:84 | ||||
chr17:5420080-5420225 | Rare:59 | ||||
chr17:5486157-5486533 | Common:4; Rare:130 | ||||
chr17:6640646-6641070 | Common:7; Rare:126 |