| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:34425984-34426231 | Common:5; Rare:104; Clinvar:1; Clinvar (benign):8 | ||||
| chr6:34696768-34697018 | Common:1; Rare:56 | ||||
| chr6:34757379-34757586 | Rare:65 | ||||
| chr6:34791980-34792131 | Common:3; Rare:46 | ||||
| chr6:34887935-34888124 | Common:1; Rare:49 | ||||
| chr6:35259396-35259772 | Common:3; Rare:118 | ||||
| chr6:35342332-35342625 | Common:1; Rare:83 | ||||
| chr6:35468209-35468466 | Common:3; Rare:97 | ||||
| chr6:35468692-35468870 | Common:2; Rare:51 | ||||
| chr6:35688849-35689171 | Common:1; Rare:107 | ||||
| chr6:35728295-35728422 | Rare:22 | ||||
| chr6:35921035-35921261 | Common:2; Rare:94 | ||||
| chr6:36197200-36197396 | Rare:72 | ||||
| chr6:36442833-36443083 | Common:2; Rare:92 | ||||
| chr6:36547315-36547601 | Common:1; Rare:122 |