Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:94062904-94063093 | Rare:45 | ||||
chr3:97764496-97764802 | Common:1; Rare:67; Clinvar:1; Clinvar (benign):1 | ||||
chr3:97972385-97972534 | Common:3; Rare:56 | ||||
chr3:98732121-98732288 | Rare:22 | ||||
chr3:98732410-98732512 | Rare:18 | ||||
chr3:98732610-98732812 | Rare:43 | ||||
chr3:99638503-99638658 | Common:1; Rare:35 | ||||
chr3:99817562-99817962 | Rare:124 | ||||
chr3:99876107-99876269 | Common:1; Rare:42 | ||||
chr3:100159617-100159881 | Rare:50 | ||||
chr3:100260704-100261039 | Rare:93 | ||||
chr3:100401357-100401576 | Common:1; Rare:51 | ||||
chr3:101513136-101513212 | Rare:22 | ||||
chr3:101561746-101561966 | Common:2; Rare:82 | ||||
chr3:101573995-101574240 | Rare:85 |