| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:5260649-5261055 | Common:5; Rare:147; Clinvar (benign):4 | ||||
| chr6:5261236-5261591 | Common:9; Rare:99 | ||||
| chr6:6320618-6320734 | Rare:35 | ||||
| chr6:7107449-7108063 | Common:3; Rare:190 | ||||
| chr6:7108577-7108670 | Rare:32 | ||||
| chr6:7139069-7139256 | Rare:34 | ||||
| chr6:7313045-7313266 | Common:5; Rare:89 | ||||
| chr6:7389362-7389495 | Rare:27 | ||||
| chr6:7389708-7390080 | Common:2; Rare:117 | ||||
| chr6:7590149-7590277 | Common:2; Rare:54 | ||||
| chr6:8064332-8064472 | Common:4; Rare:55 | ||||
| chr6:8101994-8102200 | Common:3; Rare:38 | ||||
| chr6:8102452-8102749 | Common:1; Rare:104 | ||||
| chr6:8435440-8435726 | Common:7; Rare:102 | ||||
| chr6:8435829-8435893 | Common:1; Rare:16 |