Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:14953994-14954201 | Rare:75 | ||||
chr10:15860453-15860572 | Rare:34 | ||||
chr10:16436831-16437042 | Common:1; Rare:46 | ||||
chr10:16817473-16817851 | Common:1; Rare:116 | ||||
chr10:17228463-17228675 | Common:1; Rare:57 | ||||
chr10:17228995-17229026 | Rare:6 | ||||
chr10:17643877-17644293 | Common:2; Rare:125 | ||||
chr10:18651582-18651720 | Common:1; Rare:56 | ||||
chr10:18659103-18659352 | Common:2; Rare:76 | ||||
chr10:24466416-24466551 | Rare:22 | ||||
chr10:27100461-27100630 | Common:4; Rare:49; Clinvar:2; Clinvar (benign):2 | ||||
chr10:27154315-27154474 | Rare:42 | ||||
chr10:27155161-27155426 | Common:7; Rare:112; Clinvar:5; Clinvar (benign):7 | ||||
chr10:27242058-27242223 | Common:1; Rare:69 | ||||
chr10:27504041-27504382 | Rare:154; Clinvar:4; Clinvar (benign):1 |