Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:100261322-100261565 | Common:1; Rare:44 | ||||
chr3:100334672-100334780 | Common:1; Rare:50 | ||||
chr3:100401407-100401594 | Common:1; Rare:32 | ||||
chr3:100492482-100492658 | Rare:51 | ||||
chr3:100709235-100709718 | Common:6; Rare:146; Clinvar (benign):1 | ||||
chr3:101561777-101561921 | Common:2; Rare:45 | ||||
chr3:101574005-101574279 | Common:1; Rare:99 | ||||
chr3:101677074-101677171 | Rare:43 | ||||
chr3:101686480-101686896 | Common:2; Rare:164 | ||||
chr3:101724531-101724650 | Rare:43 | ||||
chr3:101779141-101779253 | Common:3; Rare:32 | ||||
chr3:105366714-105366919 | Common:2; Rare:54 | ||||
chr3:105868784-105869193 | Common:7; Rare:136 | ||||
chr3:107598976-107599071 | Rare:15 | ||||
chr3:108222180-108222593 | Common:2; Rare:132 |