Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:107035736-107035920 | Common:3; Rare:45 | ||||
chr4:108620391-108620622 | Common:6; Rare:116 | ||||
chr4:109433753-109433870 | Common:1; Rare:47 | ||||
chr4:109560167-109560316 | Rare:50 | ||||
chr4:112145291-112145482 | Common:1; Rare:49 | ||||
chr4:112285761-112285976 | Rare:65 | ||||
chr4:112636898-112637181 | Rare:75 | ||||
chr4:113761123-113761438 | Common:2; Rare:69 | ||||
chr4:118352730-118352883 | Common:2; Rare:52; Clinvar (benign):1 | ||||
chr4:118685355-118685465 | Common:2; Rare:39 | ||||
chr4:119212355-119212730 | Common:3; Rare:117 | ||||
chr4:120066748-120066911 | Common:2; Rare:52 | ||||
chr4:121696868-121697098 | Common:5; Rare:68 | ||||
chr4:122922901-122923083 | Common:2; Rare:33 | ||||
chr4:128287479-128287559 | Common:1; Rare:32 |