Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:2999637-2999995 | Common:10; Rare:75 | ||||
chr6:3063809-3063968 | Common:1; Rare:62 | ||||
chr6:3118337-3118393 | Common:1; Rare:27 | ||||
chr6:3118559-3118781 | Common:3; Rare:76 | ||||
chr6:3157417-3157669 | Common:6; Rare:82; Clinvar (benign):1 | ||||
chr6:3227592-3228037 | Rare:112 | ||||
chr6:3230906-3231238 | Common:2; Rare:74 | ||||
chr6:3231290-3231397 | Common:1; Rare:28 | ||||
chr6:3231700-3231994 | Rare:54 | ||||
chr6:3258765-3259101 | Rare:128 | ||||
chr6:4021185-4021454 | Rare:116 | ||||
chr6:5003610-5003778 | Common:5; Rare:49 | ||||
chr6:5004006-5004084 | Rare:40 | ||||
chr6:5260661-5261071 | Common:6; Rare:149; Clinvar (benign):4 | ||||
chr6:5261253-5261618 | Common:10; Rare:105 |