Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:17643834-17644309 | Common:2; Rare:155 | ||||
chr10:17644623-17644715 | Rare:16 | ||||
chr10:18140254-18140458 | Common:3; Rare:47 | ||||
chr10:18140542-18140629 | Rare:25 | ||||
chr10:18140641-18140959 | Common:2; Rare:121; Clinvar:5; Clinvar (benign):9 | ||||
chr10:18140976-18141111 | Common:2; Rare:23 | ||||
chr10:18651416-18651833 | Common:1; Rare:146 | ||||
chr10:18658659-18659006 | Common:1; Rare:90 | ||||
chr10:18659032-18659596 | Common:4; Rare:170 | ||||
chr10:18659728-18659858 | Rare:33 | ||||
chr10:19815686-19815893 | Rare:58 | ||||
chr10:19815928-19816654 | Common:8; Rare:172 | ||||
chr10:21173862-21174018 | Common:3; Rare:39 | ||||
chr10:21174028-21174712 | Common:4; Rare:171 | ||||
chr10:21496751-21496881 | Rare:37 |