Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:179858797-179858969 | Rare:96 | ||||
chr5:180810095-180810289 | Common:5; Rare:60 | ||||
chr5:181243735-181243960 | Common:4; Rare:87 | ||||
chr5:181261124-181261223 | Rare:27 | ||||
chr6:693054-693169 | Rare:42 | ||||
chr6:1389419-1389786 | Rare:81 | ||||
chr6:2245575-2245825 | Rare:86 | ||||
chr6:3068248-3068606 | Common:1; Rare:115 | ||||
chr6:3157532-3157656 | Common:6; Rare:48 | ||||
chr6:4021213-4021466 | Rare:110 | ||||
chr6:5003649-5003834 | Common:5; Rare:57 | ||||
chr6:5260675-5261060 | Common:6; Rare:138; Clinvar (benign):4 | ||||
chr6:5261224-5261585 | Common:11; Rare:97 | ||||
chr6:7313109-7313262 | Common:4; Rare:62 | ||||
chr6:7541351-7541567 | Common:1; Rare:70 |