| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43076836-43077312 | Common:5; Rare:156 | ||||
| chr6:43170722-43170847 | Rare:18 | ||||
| chr6:43170949-43171312 | Common:1; Rare:91 | ||||
| chr6:43181730-43181950 | Common:2; Rare:35 | ||||
| chr6:43182089-43182218 | Rare:34 | ||||
| chr6:43229324-43229556 | Rare:77 | ||||
| chr6:43247120-43247660 | Rare:110 | ||||
| chr6:43247695-43248095 | Common:3; Rare:114 | ||||
| chr6:43368786-43369015 | Common:1; Rare:70 | ||||
| chr6:43369457-43369894 | Common:3; Rare:143 | ||||
| chr6:43427749-43427908 | Rare:39 | ||||
| chr6:43477406-43477647 | Rare:59 | ||||
| chr6:43510240-43510550 | Common:4; Rare:96 | ||||
| chr6:43516857-43517137 | Common:4; Rare:109; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575941-43576223 | Common:1; Rare:115; Clinvar:7 |