Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:39056917-39057058 | Common:4; Rare:41 | ||||
chr17:41678756-41679012 | Common:2; Rare:46 | ||||
chr17:42574152-42574370 | Common:1; Rare:69; Clinvar:1 | ||||
chr17:42613976-42614289 | Rare:84; Clinvar (benign):1 | ||||
chr17:43010853-43011062 | Rare:34 | ||||
chr17:43315650-43315923 | Common:7; Rare:118 | ||||
chr17:43368067-43368367 | Common:10; Rare:127 | ||||
chr17:43388282-43388667 | Common:11; Rare:69 | ||||
chr17:45147415-45147554 | Common:1; Rare:24 | ||||
chr17:45247776-45247975 | Common:1; Rare:33 | ||||
chr17:45585169-45585330 | Rare:22 | ||||
chr17:46266813-46267108 | Common:16; Rare:67 | ||||
chr17:47100271-47100422 | Common:1; Rare:39 | ||||
chr17:47492455-47492763 | Common:2; Rare:99 | ||||
chr17:48002602-48002798 | Rare:27 |