Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:120408221-120408308 | Common:1; Rare:11 | ||||
chr3:120425390-120425778 | Common:1; Rare:79 | ||||
chr3:120434385-120434611 | Common:2; Rare:41 | ||||
chr3:120448829-120448981 | Rare:21 | ||||
chr3:120598635-120598832 | Common:2; Rare:26 | ||||
chr3:120598942-120598947 | |||||
chr3:120599086-120599295 | Rare:37 | ||||
chr3:121714582-121714894 | Rare:40 | ||||
chr3:121731428-121731499 | Common:1; Rare:10 | ||||
chr3:122414550-122414563 | Rare:2 | ||||
chr3:122436865-122437193 | Rare:76 | ||||
chr3:122725121-122725428 | Common:2; Rare:74 | ||||
chr3:123618636-123618919 | Rare:89; Clinvar:7; Clinvar (benign):3 | ||||
chr3:123650622-123650727 | Common:1; Rare:17 | ||||
chr3:123737541-123737729 | Common:1; Rare:51 |