Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:15431162-15431451 | Common:5; Rare:55 | ||||
chr17:15434308-15434644 | Common:2; Rare:62 | ||||
chr17:16822547-16822851 | Common:5; Rare:28 | ||||
chr17:17683390-17683668 | Rare:57 | ||||
chr17:17836196-17836418 | Common:3; Rare:62 | ||||
chr17:18449890-18450183 | Common:2; Rare:36 | ||||
chr17:18961744-18961946 | Common:1; Rare:42 | ||||
chr17:20300824-20301030 | Rare:31 | ||||
chr17:20920923-20921077 | Common:1; Rare:32 | ||||
chr17:21286439-21286625 | Common:2; Rare:35 | ||||
chr17:28339159-28339452 | Rare:68 | ||||
chr17:31560161-31560281 | Rare:26 | ||||
chr17:31596844-31596939 | Rare:17 | ||||
chr17:38465711-38465833 | Common:1; Rare:28 | ||||
chr17:40456280-40456674 | Rare:96; Clinvar (pathogenic):1 |