Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:75435067-75435378 | Common:3; Rare:109 | ||||
chr3:81761523-81761609 | Common:5; Rare:25; Clinvar (benign):1 | ||||
chr3:98961782-98961930 | Rare:20 | ||||
chr3:101676254-101676474 | Common:2; Rare:73 | ||||
chr3:104440025-104440287 | Rare:69 | ||||
chr3:105368762-105368961 | Common:1; Rare:32 | ||||
chr3:107240624-107240739 | Rare:49 | ||||
chr3:115784625-115784757 | Common:1; Rare:34 | ||||
chr3:115790872-115791035 | Common:2; Rare:25 | ||||
chr3:118810797-118810903 | Rare:46 | ||||
chr3:119184832-119185087 | Rare:51 | ||||
chr3:120095056-120095249 | Rare:56 | ||||
chr3:149388057-149388288 | Common:2; Rare:41 | ||||
chr3:150408860-150408988 | Rare:38 | ||||
chr3:157081642-157081784 | Common:1; Rare:20 |