Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:15748110-15748344 | Common:2; Rare:48; Clinvar:4; Clinvar (benign):4 | ||||
chr16:15759649-15759836 | Common:1; Rare:47; Clinvar:3; Clinvar (benign):4 | ||||
chr16:21820402-21820557 | Rare:48 | ||||
chr17:7887466-7887788 | Rare:63 | ||||
chr17:8477044-8477145 | Common:1; Rare:34 | ||||
chr17:17836191-17836412 | Common:2; Rare:62 | ||||
chr17:44797748-44797917 | Rare:27 | ||||
chr17:50197699-50197858 | Common:1; Rare:44; Clinvar:3 | ||||
chr17:59673556-59673752 | Common:1; Rare:42 | ||||
chr17:59838561-59838739 | Rare:30 | ||||
chr17:64975561-64975718 | Common:1; Rare:52 | ||||
chr17:76557669-76557834 | Common:1; Rare:55 | ||||
chr17:80109748-80109894 | Common:2; Rare:38 | ||||
chr18:3593835-3594127 | Common:3; Rare:46 | ||||
chr18:3594277-3594462 | Rare:37 |