Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:105037894-105038110 | Common:3; Rare:76 | ||||
chr2:105337468-105337620 | Common:1; Rare:71 | ||||
chr2:106194278-106194568 | Common:4; Rare:112 | ||||
chr2:106887255-106887314 | Rare:13 | ||||
chr2:108449097-108449239 | Rare:46 | ||||
chr2:108534204-108534477 | Common:7; Rare:113 | ||||
chr2:108719352-108719619 | Common:3; Rare:117; Clinvar (benign):2 | ||||
chr2:109613865-109614008 | Common:2; Rare:50 | ||||
chr2:111884132-111884262 | Rare:38 | ||||
chr2:111898305-111898706 | Common:3; Rare:88; Clinvar (benign):1 | ||||
chr2:112275394-112275637 | Common:1; Rare:82 | ||||
chr2:112584393-112584654 | Common:1; Rare:74 | ||||
chr2:112645701-112646019 | Common:1; Rare:122 | ||||
chr2:113627041-113627303 | Common:3; Rare:78 | ||||
chr2:113756522-113756781 | Common:3; Rare:86 |