| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:5260679-5261010 | Common:3; Rare:113; Clinvar (benign):4 | ||||
| chr6:7389732-7389881 | Common:1; Rare:44 | ||||
| chr6:7590077-7590258 | Common:5; Rare:57 | ||||
| chr6:8435496-8435659 | Common:3; Rare:61 | ||||
| chr6:10412145-10412325 | Rare:63 | ||||
| chr6:10694583-10694994 | Common:5; Rare:118 | ||||
| chr6:10722808-10723220 | Common:6; Rare:138 | ||||
| chr6:10747614-10747869 | Common:2; Rare:102 | ||||
| chr6:11232658-11232787 | Rare:26 | ||||
| chr6:13615184-13615458 | Common:2; Rare:117 | ||||
| chr6:13615507-13615600 | Rare:31 | ||||
| chr6:16761444-16761758 | Common:2; Rare:96 | ||||
| chr6:17393472-17393720 | Common:1; Rare:69 | ||||
| chr6:20403579-20403723 | Common:1; Rare:37 | ||||
| chr6:20534392-20534525 | Rare:44 |