Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:17258269-17258451 | Common:3; Rare:31 | ||||
chr22:22298040-22298196 | Common:2; Rare:67 | ||||
chr22:25447963-25448131 | Common:3; Rare:54 | ||||
chr22:26657480-26657643 | Common:1; Rare:28 | ||||
chr22:27800817-27800845 | Rare:6 | ||||
chr22:41867138-41867412 | Rare:72 | ||||
chr22:41951964-41952171 | Common:3; Rare:45 | ||||
chr22:42601138-42601231 | Rare:21 | ||||
chr22:46069860-46070067 | Rare:46 | ||||
chr3:11412131-11412316 | Common:2; Rare:35 | ||||
chr3:40453171-40453417 | Common:5; Rare:53 | ||||
chr3:43999111-43999386 | Rare:88 | ||||
chr3:71064163-71064261 | Common:2; Rare:25 | ||||
chr3:75434995-75435377 | Common:5; Rare:132 | ||||
chr3:81761513-81761597 | Common:5; Rare:26; Clinvar (benign):1 |