Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:97821794-97822074 | Rare:96 | ||||
chr3:98732344-98732508 | Rare:31 | ||||
chr3:99638357-99638624 | Common:1; Rare:60 | ||||
chr3:99817562-99817904 | Rare:98 | ||||
chr3:99876107-99876278 | Common:1; Rare:43 | ||||
chr3:100114356-100114941 | Common:3; Rare:106 | ||||
chr3:100260691-100261057 | Rare:106 | ||||
chr3:100334677-100334780 | Common:1; Rare:47 | ||||
chr3:100401398-100401580 | Common:1; Rare:34 | ||||
chr3:100492480-100492668 | Rare:54 | ||||
chr3:100709250-100709628 | Common:6; Rare:125; Clinvar (benign):1 | ||||
chr3:101513122-101513321 | Common:8; Rare:41 | ||||
chr3:101573981-101574225 | Rare:84 | ||||
chr3:101677082-101677185 | Rare:43 | ||||
chr3:101686485-101686870 | Common:2; Rare:156 |