| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:52284682-52285041 | Common:2; Rare:128 | ||||
| chr6:52420110-52420385 | Common:3; Rare:114; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:52576987-52577292 | Common:5; Rare:114 | ||||
| chr6:52671054-52671190 | Rare:37 | ||||
| chr6:52995267-52995832 | Common:4; Rare:230 | ||||
| chr6:53061690-53061935 | Rare:58 | ||||
| chr6:53065379-53065470 | Common:1; Rare:29 | ||||
| chr6:53065515-53065656 | Rare:33 | ||||
| chr6:53065705-53065745 | Rare:12 | ||||
| chr6:53348493-53348621 | Rare:30 | ||||
| chr6:53348847-53349241 | Common:2; Rare:162 | ||||
| chr6:53794248-53794514 | Common:4; Rare:48 | ||||
| chr6:53929751-53930047 | Common:2; Rare:53 | ||||
| chr6:54846559-54846805 | Common:1; Rare:61 | ||||
| chr6:56541111-56541145 | Rare:3 |