| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:2999562-2999912 | Common:11; Rare:79 | ||||
| chr6:3068343-3068630 | Common:2; Rare:98 | ||||
| chr6:3118602-3118789 | Common:3; Rare:66 | ||||
| chr6:3157471-3157629 | Common:6; Rare:65 | ||||
| chr6:3231733-3231824 | Rare:16 | ||||
| chr6:4021224-4021466 | Rare:107 | ||||
| chr6:5003609-5003836 | Common:6; Rare:70 | ||||
| chr6:5003974-5004141 | Common:2; Rare:69 | ||||
| chr6:5260661-5261656 | Common:21; Rare:312; Clinvar (benign):4 | ||||
| chr6:7389740-7390059 | Common:1; Rare:92 | ||||
| chr6:7541307-7541867 | Common:3; Rare:156; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:7910777-7911013 | Rare:80 | ||||
| chr6:8435392-8435646 | Common:3; Rare:89 | ||||
| chr6:10412113-10412326 | Common:1; Rare:73 | ||||
| chr6:10412330-10412552 | Common:1; Rare:41 |