Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:10697503-10697654 | Common:3; Rare:59; Clinvar:2; Clinvar (benign):2 | ||||
chr17:14069440-14069549 | Common:2; Rare:37; Clinvar:1; Clinvar (benign):2 | ||||
chr17:15699514-15699763 | Common:3; Rare:63 | ||||
chr17:15999703-16000003 | Common:2; Rare:114; Clinvar:4; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
chr17:17281194-17281397 | Rare:82 | ||||
chr17:17591573-17591932 | Common:2; Rare:105 | ||||
chr17:18314964-18315297 | Rare:99 | ||||
chr17:19977816-19977950 | Common:1; Rare:43 | ||||
chr17:21214139-21214372 | Common:2; Rare:106 | ||||
chr17:27293979-27294122 | Common:1; Rare:60 | ||||
chr17:28335445-28335811 | Common:1; Rare:82 | ||||
chr17:28357455-28357679 | Common:5; Rare:112 | ||||
chr17:28662166-28662290 | Rare:52 | ||||
chr17:28854971-28855026 | Rare:14 | ||||
chr17:29294108-29294365 | Common:3; Rare:101 |