Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:17228916-17229026 | Common:1; Rare:29 | ||||
chr10:17229114-17229298 | Common:1; Rare:34 | ||||
chr10:17230416-17230710 | Common:1; Rare:106; Clinvar:1 | ||||
chr10:17643871-17644274 | Common:2; Rare:121 | ||||
chr10:18651564-18651668 | Common:1; Rare:40 | ||||
chr10:18659103-18659362 | Common:2; Rare:78 | ||||
chr10:19815719-19815862 | Rare:41 | ||||
chr10:19816270-19816647 | Common:6; Rare:83 | ||||
chr10:21526378-21526568 | Common:1; Rare:61 | ||||
chr10:22316255-22316459 | Rare:92 | ||||
chr10:24466408-24466679 | Rare:43 | ||||
chr10:24722704-24722846 | Common:1; Rare:37 | ||||
chr10:25016353-25016661 | Common:8; Rare:103 | ||||
chr10:27154310-27154480 | Rare:45 | ||||
chr10:27155161-27155423 | Common:7; Rare:111; Clinvar:5; Clinvar (benign):7 |