Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:108074691-108074831 | Rare:36; Clinvar:1 | ||||
chr6:108560726-108560984 | Rare:107 | ||||
chr6:108848141-108848475 | Common:1; Rare:104 | ||||
chr6:109009446-109009682 | Common:2; Rare:75 | ||||
chr6:109094445-109094597 | Rare:33 | ||||
chr6:109095412-109095551 | Rare:29 | ||||
chr6:109382365-109382806 | Common:5; Rare:150; Clinvar (benign):1 | ||||
chr6:109440575-109440724 | Rare:48 | ||||
chr6:109691158-109691322 | Common:3; Rare:40; Clinvar:4; Clinvar (benign):3 | ||||
chr6:110415525-110415651 | Rare:27 | ||||
chr6:110958672-110958764 | Common:1; Rare:38 | ||||
chr6:110981950-110982106 | Common:2; Rare:79 | ||||
chr6:112087424-112087684 | Rare:85 | ||||
chr6:113857268-113857395 | Common:1; Rare:27 | ||||
chr6:116100695-116100909 | Common:1; Rare:80 |