Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:101576982-101576999 | Rare:3 | ||||
chr3:107240636-107240729 | Rare:42 | ||||
chr3:114872748-114872872 | Common:1; Rare:18 | ||||
chr3:120642876-120642906 | Rare:3 | ||||
chr3:122427610-122427814 | Rare:45 | ||||
chr3:123626820-123627083 | Common:1; Rare:49; Clinvar:5; Clinvar (benign):3 | ||||
chr3:123734174-123734264 | Common:1; Rare:12; Clinvar:1; Clinvar (benign):2 | ||||
chr3:124700988-124701249 | Common:1; Rare:51 | ||||
chr3:124812851-124813039 | Common:2; Rare:28 | ||||
chr3:124835054-124835261 | Common:3; Rare:45 | ||||
chr3:126125655-126126015 | Common:1; Rare:53 | ||||
chr3:126355982-126356234 | Rare:69 | ||||
chr3:126468312-126468535 | Common:2; Rare:43 | ||||
chr3:126472265-126472582 | Rare:56 | ||||
chr3:127785242-127785337 | Rare:21 |