Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:41812859-41813029 | Rare:45 | ||||
chr17:42577639-42577844 | Rare:99 | ||||
chr17:45061119-45061329 | Common:1; Rare:59 | ||||
chr17:46923093-46923172 | Common:1; Rare:32; Clinvar (benign):6 | ||||
chr17:47831516-47831653 | Rare:35 | ||||
chr17:48944781-48944898 | Common:1; Rare:35 | ||||
chr17:50373160-50373254 | Common:3; Rare:42 | ||||
chr17:51260362-51260576 | Common:3; Rare:95 | ||||
chr17:54968638-54968769 | Common:3; Rare:63 | ||||
chr17:56914038-56914177 | Rare:31 | ||||
chr17:57084992-57085316 | Rare:111 | ||||
chr17:57850013-57850285 | Common:1; Rare:84 | ||||
chr17:58007218-58007384 | Common:1; Rare:71 | ||||
chr17:58692559-58692650 | Common:1; Rare:50; Clinvar:5; Clinvar (benign):16 | ||||
chr17:59106715-59106993 | Common:2; Rare:93; Clinvar:4; Clinvar (benign):2 |