Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:1829812-1830082 | Common:7; Rare:114 | ||||
chr17:2303293-2303357 | Rare:18 | ||||
chr17:2303504-2303631 | Rare:47 | ||||
chr17:2303724-2303987 | Common:2; Rare:99 | ||||
chr17:2336420-2336543 | Rare:49 | ||||
chr17:2511806-2512031 | Common:2; Rare:70 | ||||
chr17:2593464-2593664 | Common:2; Rare:77 | ||||
chr17:3636241-3636468 | Common:4; Rare:61; Clinvar (benign):1 | ||||
chr17:3668552-3668853 | Common:2; Rare:121 | ||||
chr17:3723764-3723932 | Common:1; Rare:96 | ||||
chr17:3892952-3893254 | Common:3; Rare:103 | ||||
chr17:4143042-4143244 | Rare:63 | ||||
chr17:4143605-4143735 | Common:4; Rare:76 | ||||
chr17:4187107-4187382 | Common:1; Rare:54 | ||||
chr17:4555326-4555483 | Common:2; Rare:67 |