Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:2971551-2971721 | Common:1; Rare:47 | ||||
chr6:2999633-2999903 | Common:10; Rare:58 | ||||
chr6:3118605-3118737 | Common:2; Rare:43 | ||||
chr6:4021238-4021415 | Rare:86 | ||||
chr6:5004007-5004102 | Common:1; Rare:48 | ||||
chr6:5260694-5261025 | Common:3; Rare:109; Clinvar (benign):4 | ||||
chr6:7389740-7389881 | Common:1; Rare:41 | ||||
chr6:7541374-7541676 | Common:1; Rare:93; Clinvar (benign):1 | ||||
chr6:8435481-8435659 | Common:3; Rare:71 | ||||
chr6:10694603-10694988 | Common:4; Rare:103 | ||||
chr6:10722965-10723220 | Common:4; Rare:98 | ||||
chr6:10747582-10747869 | Common:3; Rare:110 | ||||
chr6:11232633-11232787 | Rare:31 | ||||
chr6:13328509-13328609 | Common:2; Rare:37 | ||||
chr6:13615170-13615490 | Common:2; Rare:136 |