| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:5691686-5691835 | Common:3; Rare:38 | ||||
| chr2:5691836-5692041 | Common:4; Rare:58 | ||||
| chr2:5693422-5693472 | Rare:23; Clinvar (benign):1 | ||||
| chr2:5694481-5694533 | Rare:12 | ||||
| chr2:5696020-5696344 | Rare:80 | ||||
| chr2:5696559-5696677 | Rare:34 | ||||
| chr2:5696809-5696982 | Rare:68 | ||||
| chr2:5697008-5697154 | Common:3; Rare:52 | ||||
| chr2:5697231-5697354 | Common:2; Rare:38 | ||||
| chr2:5697360-5697641 | Common:2; Rare:64 | ||||
| chr2:5726027-5726242 | Common:1; Rare:47 | ||||
| chr2:5726379-5726449 | Rare:16 | ||||
| chr2:5803683-5803895 | Common:1; Rare:51 | ||||
| chr2:5846974-5847286 | Common:3; Rare:57 | ||||
| chr2:5914899-5915106 | Rare:36 |