| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:2841454-2841673 | Rare:52 | ||||
| chr6:2841801-2841930 | Common:1; Rare:27 | ||||
| chr6:2841933-2842038 | Rare:17 | ||||
| chr6:2971251-2971699 | Common:6; Rare:115 | ||||
| chr6:2999613-3000040 | Common:10; Rare:93 | ||||
| chr6:3118355-3118369 | Rare:5 | ||||
| chr6:3118581-3118741 | Common:2; Rare:52 | ||||
| chr6:3157511-3157663 | Common:6; Rare:56 | ||||
| chr6:3849145-3849455 | Common:3; Rare:89 | ||||
| chr6:4021187-4021453 | Rare:115 | ||||
| chr6:5003610-5003843 | Common:6; Rare:72 | ||||
| chr6:5004006-5004106 | Common:1; Rare:50 | ||||
| chr6:5260662-5261055 | Common:5; Rare:142; Clinvar (benign):4 | ||||
| chr6:5261263-5261559 | Common:9; Rare:76 | ||||
| chr6:7107812-7108455 | Common:2; Rare:184 |