Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:181261073-181261272 | Rare:67 | ||||
chr6:693050-693209 | Rare:51 | ||||
chr6:2245430-2245817 | Common:1; Rare:129 | ||||
chr6:2971263-2971709 | Common:5; Rare:115 | ||||
chr6:2999622-2999893 | Common:10; Rare:58 | ||||
chr6:3068477-3068553 | Common:1; Rare:18 | ||||
chr6:3118365-3118669 | Common:3; Rare:91 | ||||
chr6:3157532-3157676 | Common:6; Rare:54 | ||||
chr6:3258837-3259025 | Rare:72 | ||||
chr6:4021159-4021445 | Common:1; Rare:119 | ||||
chr6:5003627-5003843 | Common:6; Rare:68 | ||||
chr6:5003995-5004102 | Common:2; Rare:54 | ||||
chr6:5260720-5261025 | Common:2; Rare:95; Clinvar (benign):2 | ||||
chr6:5261274-5261553 | Common:9; Rare:68 | ||||
chr6:7313127-7313315 | Common:4; Rare:71 |