Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:4807002-4807183 | Common:3; Rare:60 | ||||
chr17:4939912-4940336 | Common:2; Rare:125 | ||||
chr17:4987635-4987734 | Common:1; Rare:40 | ||||
chr17:5420086-5420207 | Rare:48 | ||||
chr17:5486161-5486505 | Common:4; Rare:126 | ||||
chr17:6640717-6641082 | Common:7; Rare:117 | ||||
chr17:6651553-6651762 | Common:1; Rare:75 | ||||
chr17:7012301-7012680 | Rare:132 | ||||
chr17:7219764-7219957 | Common:3; Rare:83; Clinvar:5; Clinvar (benign):2 | ||||
chr17:7251940-7252319 | Common:2; Rare:152 | ||||
chr17:7352068-7352288 | Rare:72 | ||||
chr17:7484203-7484370 | Common:1; Rare:66 | ||||
chr17:7557849-7558201 | Common:4; Rare:78 | ||||
chr17:7583508-7583868 | Common:1; Rare:141; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr17:7857463-7858098 | Common:4; Rare:205 |