Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:58352134-58352458 | Common:6; Rare:128 | ||||
chr17:58692530-58692668 | Common:1; Rare:75; Clinvar:10; Clinvar (benign):20 | ||||
chr17:59106707-59107153 | Common:2; Rare:146; Clinvar:4; Clinvar (benign):2 | ||||
chr17:59155126-59155784 | Common:2; Rare:169 | ||||
chr17:59619209-59619345 | Common:1; Rare:38 | ||||
chr17:59619563-59619998 | Common:3; Rare:157 | ||||
chr17:59707397-59707727 | Common:3; Rare:90; Clinvar (benign):3 | ||||
chr17:59837635-59837970 | Rare:48 | ||||
chr17:59892709-59893149 | Rare:117 | ||||
chr17:59964715-59964802 | Common:2; Rare:39 | ||||
chr17:60391991-60392251 | Common:2; Rare:63 | ||||
chr17:60526160-60526294 | Rare:53 | ||||
chr17:62423782-62423929 | Common:1; Rare:57 | ||||
chr17:63600835-63600922 | Rare:27; Clinvar:2 | ||||
chr17:63741765-63741980 | Common:3; Rare:92 |