Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:7885177-7885346 | Rare:49 | ||||
chr17:7888715-7888819 | Rare:28 | ||||
chr17:7931906-7932248 | Common:5; Rare:94 | ||||
chr17:8176291-8176435 | Rare:53 | ||||
chr17:8248042-8248100 | Rare:34; Clinvar:2 | ||||
chr17:8249195-8249325 | Common:1; Rare:40 | ||||
chr17:8435643-8436034 | Common:5; Rare:154 | ||||
chr17:10697481-10697660 | Common:4; Rare:80; Clinvar:5; Clinvar (benign):2 | ||||
chr17:11997444-11997594 | Rare:50 | ||||
chr17:14069436-14069593 | Common:2; Rare:66; Clinvar:4; Clinvar (benign):3 | ||||
chr17:15699504-15699773 | Common:3; Rare:71 | ||||
chr17:15999593-16000003 | Common:3; Rare:182; Clinvar:5; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
chr17:17237166-17237456 | Common:4; Rare:78; Clinvar (benign):1 | ||||
chr17:17281182-17281412 | Rare:89 | ||||
chr17:17591580-17591967 | Common:2; Rare:111 |