Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:17233569-17233951 | Common:3; Rare:123; Clinvar (benign):1 | ||||
chr10:17643846-17644281 | Common:2; Rare:137 | ||||
chr10:18651565-18651741 | Common:1; Rare:76 | ||||
chr10:18659226-18659379 | Common:2; Rare:53 | ||||
chr10:19815648-19815863 | Rare:61 | ||||
chr10:19816104-19816274 | Rare:44 | ||||
chr10:19816281-19816472 | Common:5; Rare:32 | ||||
chr10:19816574-19816689 | Rare:24 | ||||
chr10:21173876-21174222 | Common:3; Rare:90 | ||||
chr10:21526331-21526576 | Common:1; Rare:72 | ||||
chr10:21533636-21533768 | Rare:23 | ||||
chr10:21533964-21534341 | Common:3; Rare:155 | ||||
chr10:22316203-22316483 | Common:3; Rare:125 | ||||
chr10:22321337-22321522 | Rare:65 | ||||
chr10:24209005-24209193 | Rare:55 |