Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:29212504-29212845 | Rare:58 | ||||
chr17:31008551-31008638 | Common:2; Rare:25 | ||||
chr17:35567987-35568153 | Common:1; Rare:49 | ||||
chr17:38257233-38257620 | Common:1; Rare:121 | ||||
chr17:38451902-38452088 | Rare:37 | ||||
chr17:38452356-38452492 | Common:1; Rare:20 | ||||
chr17:38702306-38702479 | Rare:61 | ||||
chr17:40108220-40108474 | Rare:56 | ||||
chr17:41395156-41395316 | Common:1; Rare:51 | ||||
chr17:41502641-41503108 | Common:4; Rare:153; Clinvar:4; Clinvar (benign):8 | ||||
chr17:41503112-41503960 | Common:6; Rare:234; Clinvar:2; Clinvar (benign):5 | ||||
chr17:41511173-41511438 | Rare:55 | ||||
chr17:41515883-41516343 | Rare:160 | ||||
chr17:41516514-41517269 | Common:2; Rare:228 | ||||
chr17:41579642-41579776 | Common:1; Rare:31 |