Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:2971561-2971625 | Rare:15 | ||||
chr6:2971627-2971717 | Common:1; Rare:28 | ||||
chr6:2999607-3000006 | Common:10; Rare:85 | ||||
chr6:3068496-3068585 | Common:1; Rare:25 | ||||
chr6:3118591-3118779 | Common:3; Rare:66 | ||||
chr6:3157532-3157613 | Common:5; Rare:36 | ||||
chr6:4021200-4021437 | Rare:104 | ||||
chr6:5260681-5261013 | Common:3; Rare:113; Clinvar (benign):4 | ||||
chr6:7313049-7313285 | Common:5; Rare:92 | ||||
chr6:7541407-7541678 | Rare:82; Clinvar (benign):1 | ||||
chr6:8435472-8435690 | Common:5; Rare:84 | ||||
chr6:10694614-10694984 | Common:4; Rare:95 | ||||
chr6:10722848-10723235 | Common:6; Rare:131 | ||||
chr6:10747617-10747860 | Common:2; Rare:97 | ||||
chr6:11232497-11232709 | Rare:65 |