Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:115110857-115111169 | Common:3; Rare:60 | ||||
chr9:115116244-115116367 | Rare:21 | ||||
chr9:115650204-115650395 | Common:1; Rare:38 | ||||
chr9:115939461-115939552 | Rare:16 | ||||
chr9:115939560-115939622 | Rare:20 | ||||
chr9:116277293-116277472 | Common:3; Rare:38 | ||||
chr9:117180666-117180858 | Rare:39 | ||||
chr9:120722605-120722868 | Common:1; Rare:34 | ||||
chr9:120833354-120833636 | Rare:62 | ||||
chr9:121173492-121173738 | Common:2; Rare:78 | ||||
chr9:121284680-121284690 | Rare:2 | ||||
chr9:121310433-121310770 | Common:1; Rare:78; Clinvar (benign):1 | ||||
chr9:121318435-121318689 | Common:1; Rare:60 | ||||
chr9:121963656-121963956 | Common:3; Rare:46 | ||||
chr9:124353629-124353965 | Common:4; Rare:80 |