Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:99817568-99817928 | Rare:107 | ||||
chr3:99876116-99876269 | Common:1; Rare:39 | ||||
chr3:100260704-100261028 | Rare:86 | ||||
chr3:100401402-100401580 | Common:1; Rare:33 | ||||
chr3:100492420-100492668 | Common:2; Rare:81 | ||||
chr3:100709207-100709716 | Common:9; Rare:153; Clinvar (benign):1 | ||||
chr3:101561759-101561919 | Common:1; Rare:56 | ||||
chr3:101574005-101574225 | Rare:77 | ||||
chr3:101686619-101686904 | Common:2; Rare:115 | ||||
chr3:108222344-108222656 | Common:2; Rare:90 | ||||
chr3:108589615-108589726 | Common:1; Rare:27 | ||||
chr3:111859060-111859278 | Common:7; Rare:41 | ||||
chr3:112561609-112561748 | Rare:42 | ||||
chr3:113515122-113515257 | Rare:41 | ||||
chr3:113746172-113746392 | Rare:91 |