Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:98608447-98608636 | Common:1; Rare:82 | ||||
chr2:99180985-99181152 | Common:2; Rare:59 | ||||
chr2:105337468-105337578 | Common:1; Rare:51 | ||||
chr2:105438494-105438636 | Rare:34 | ||||
chr2:112584393-112584628 | Common:1; Rare:64 | ||||
chr2:113627040-113627266 | Common:1; Rare:65 | ||||
chr2:113889765-113890165 | Common:8; Rare:129 | ||||
chr2:119366804-119367025 | Common:1; Rare:57 | ||||
chr2:127294133-127294199 | Common:2; Rare:17; Clinvar (benign):2 | ||||
chr2:127811145-127811258 | Rare:35 | ||||
chr2:130181581-130181760 | Common:2; Rare:81 | ||||
chr2:131105192-131105351 | Common:1; Rare:67 | ||||
chr2:134918597-134918852 | Common:1; Rare:101 | ||||
chr2:135531219-135531476 | Common:1; Rare:37 | ||||
chr2:149587299-149587434 | Common:1; Rare:32 |