Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:3668534-3668820 | Common:3; Rare:114 | ||||
chr17:4142954-4143206 | Common:3; Rare:91 | ||||
chr17:4143608-4143748 | Common:4; Rare:82 | ||||
chr17:4263943-4264069 | Rare:50 | ||||
chr17:4704101-4704245 | Rare:77 | ||||
chr17:4807002-4807165 | Common:3; Rare:53 | ||||
chr17:4939906-4940107 | Common:1; Rare:67 | ||||
chr17:5486317-5486573 | Common:4; Rare:67 | ||||
chr17:6651570-6651709 | Common:1; Rare:51 | ||||
chr17:7012326-7012681 | Rare:121 | ||||
chr17:7251925-7252286 | Common:2; Rare:137 | ||||
chr17:7351963-7352196 | Rare:68 | ||||
chr17:7484215-7484371 | Common:1; Rare:62 | ||||
chr17:7583736-7583860 | Common:1; Rare:59; Clinvar:1; Clinvar (benign):3 | ||||
chr17:7931902-7932253 | Common:5; Rare:95 |