Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:123629587-123629657 | Rare:18; Clinvar (benign):1 | ||||
chr3:125916318-125916615 | Common:4; Rare:89 | ||||
chr3:125990535-125990588 | Common:1; Rare:14 | ||||
chr3:130111461-130111753 | Common:3; Rare:72 | ||||
chr3:130112407-130112589 | Common:3; Rare:56 | ||||
chr3:131361598-131361938 | Common:3; Rare:104 | ||||
chr3:141660252-141660377 | Rare:39 | ||||
chr3:146242071-146242202 | Rare:26 | ||||
chr3:150408860-150409029 | Rare:49 | ||||
chr3:150761846-150761937 | Common:1; Rare:14 | ||||
chr3:151539193-151539306 | Common:1; Rare:31 | ||||
chr3:151770109-151770427 | Common:4; Rare:50 | ||||
chr3:155737851-155738050 | Common:1; Rare:21 | ||||
chr3:156816986-156817363 | Rare:104 | ||||
chr3:157088673-157088920 | Common:1; Rare:65 |