Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:99817562-99817982 | Rare:129 | ||||
chr3:99876124-99876278 | Common:1; Rare:39 | ||||
chr3:100260701-100261057 | Rare:104 | ||||
chr3:100334501-100334786 | Common:2; Rare:87 | ||||
chr3:100401383-100401576 | Common:1; Rare:41 | ||||
chr3:100492420-100492913 | Common:11; Rare:122 | ||||
chr3:100709214-100709716 | Common:9; Rare:152; Clinvar (benign):1 | ||||
chr3:101513135-101513353 | Common:8; Rare:50 | ||||
chr3:101561746-101561976 | Common:2; Rare:86 | ||||
chr3:101573996-101574244 | Rare:88 | ||||
chr3:101677082-101677157 | Rare:35 | ||||
chr3:101685819-101686165 | Common:4; Rare:87 | ||||
chr3:101724531-101724642 | Rare:38 | ||||
chr3:101779134-101779253 | Common:3; Rare:38 | ||||
chr3:105868848-105869184 | Common:6; Rare:120 |