Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:97764706-97764795 | Common:1; Rare:17; Clinvar (benign):1 | ||||
chr3:97821921-97822045 | Rare:46 | ||||
chr3:99638380-99638630 | Common:1; Rare:61 | ||||
chr3:99817568-99817924 | Rare:104 | ||||
chr3:99876107-99876254 | Rare:37 | ||||
chr3:100260733-100261034 | Rare:79 | ||||
chr3:100401389-100401580 | Common:1; Rare:39 | ||||
chr3:100492413-100492743 | Common:2; Rare:100 | ||||
chr3:100709235-100709378 | Common:1; Rare:52 | ||||
chr3:101574062-101574242 | Rare:64 | ||||
chr3:101677079-101677171 | Rare:40 | ||||
chr3:101686672-101686860 | Common:2; Rare:81 | ||||
chr3:101724531-101724619 | Rare:26 | ||||
chr3:105868843-105869184 | Common:6; Rare:122 | ||||
chr3:108222344-108222571 | Common:1; Rare:56 |