Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:57084971-57085329 | Rare:122 | ||||
chr17:57850002-57850274 | Common:1; Rare:89 | ||||
chr17:58007145-58007384 | Common:1; Rare:117 | ||||
chr17:58692549-58692673 | Common:1; Rare:69; Clinvar:12; Clinvar (benign):20 | ||||
chr17:59106707-59106970 | Common:2; Rare:86; Clinvar:4; Clinvar (benign):2 | ||||
chr17:59155138-59155567 | Common:2; Rare:101 | ||||
chr17:59619569-59620010 | Common:3; Rare:157 | ||||
chr17:59707392-59707727 | Common:3; Rare:93; Clinvar (benign):4 | ||||
chr17:59837626-59837975 | Rare:49 | ||||
chr17:59892891-59893149 | Rare:76 | ||||
chr17:59964717-59965066 | Common:2; Rare:102 | ||||
chr17:60078910-60079040 | Common:5; Rare:58 | ||||
chr17:60525934-60526290 | Common:2; Rare:119 | ||||
chr17:63550153-63550536 | Common:2; Rare:88 | ||||
chr17:63773486-63773870 | Common:2; Rare:125 |