Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:143281668-143281820 | Common:1; Rare:29 | ||||
chr8:145002825-145003035 | Common:2; Rare:73 | ||||
chr9:29450769-29450960 | Common:3; Rare:71 | ||||
chr9:32550829-32551169 | Common:1; Rare:134; Clinvar:2; Clinvar (benign):2 | ||||
chr9:35737898-35737986 | Rare:33 | ||||
chr9:40992072-40992347 | Common:7; Rare:21 | ||||
chr9:66269882-66270048 | Common:2; Rare:30 | ||||
chr9:71769464-71769676 | Rare:42 | ||||
chr9:74085627-74086008 | Common:1; Rare:88 | ||||
chr9:74088097-74088136 | Common:1; Rare:6 | ||||
chr9:74088141-74088480 | Common:7; Rare:68 | ||||
chr9:74090849-74091046 | Common:1; Rare:34 | ||||
chr9:82883777-82884079 | Rare:58 | ||||
chr9:83219218-83219345 | Common:2; Rare:33 | ||||
chr9:87042044-87042182 | Rare:45 |