Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:3668571-3668820 | Common:1; Rare:96 | ||||
chr17:3723802-3723925 | Rare:68 | ||||
chr17:4263957-4264096 | Rare:54 | ||||
chr17:4555367-4555518 | Common:1; Rare:60 | ||||
chr17:4704117-4704194 | Rare:44 | ||||
chr17:4939916-4940111 | Common:1; Rare:65 | ||||
chr17:5419656-5419863 | Common:3; Rare:59 | ||||
chr17:5486169-5486399 | Common:4; Rare:96 | ||||
chr17:6640645-6641066 | Common:7; Rare:125 | ||||
chr17:6651574-6651795 | Common:1; Rare:70 | ||||
chr17:7012323-7012668 | Rare:118 | ||||
chr17:7479517-7479713 | Common:1; Rare:33 | ||||
chr17:7484241-7484370 | Common:1; Rare:52 | ||||
chr17:7583549-7583858 | Common:1; Rare:126; Clinvar:3; Clinvar (benign):3 | ||||
chr17:7931869-7932226 | Common:5; Rare:94 |