Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:180861226-180861598 | Common:4; Rare:117 | ||||
chr5:181223102-181223308 | Rare:71 | ||||
chr5:181223479-181223738 | Common:3; Rare:70 | ||||
chr5:181261054-181261286 | Rare:79 | ||||
chr6:693074-693209 | Rare:40 | ||||
chr6:1311807-1312138 | Common:3; Rare:100 | ||||
chr6:2245425-2245831 | Common:1; Rare:135 | ||||
chr6:2962131-2962238 | Common:1; Rare:17 | ||||
chr6:2999659-2999912 | Common:10; Rare:52 | ||||
chr6:3118602-3118737 | Common:2; Rare:43 | ||||
chr6:4021218-4021432 | Rare:97 | ||||
chr6:5003662-5003836 | Common:5; Rare:53 | ||||
chr6:5004007-5004102 | Common:1; Rare:48 | ||||
chr6:5260702-5261025 | Common:2; Rare:105; Clinvar (benign):2 | ||||
chr6:7107616-7107843 | Rare:88 |