Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:71112547-71112914 | Common:5; Rare:75; Clinvar:2; Clinvar (benign):1 | ||||
chr3:71244242-71244470 | Common:1; Rare:49 | ||||
chr3:73520981-73521187 | Rare:32 | ||||
chr3:73521385-73521408 | Rare:7 | ||||
chr3:73521433-73521490 | Rare:5 | ||||
chr3:73625456-73625734 | Rare:45 | ||||
chr3:75435036-75435388 | Common:5; Rare:120 | ||||
chr3:75641092-75641404 | Common:1; Rare:47 | ||||
chr3:101676275-101676517 | Common:1; Rare:84 | ||||
chr3:101851934-101852194 | Common:1; Rare:51 | ||||
chr3:107240586-107240749 | Rare:71 | ||||
chr3:112640329-112640388 | Common:1; Rare:7 | ||||
chr3:122795592-122795715 | Rare:22 | ||||
chr3:123413138-123413299 | Common:1; Rare:36 | ||||
chr3:123447440-123447574 | Common:1; Rare:46 |