| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:17752883-17753238 | Common:2; Rare:61 | ||||
| chr2:17755147-17755384 | Rare:48 | ||||
| chr2:17757272-17757382 | Rare:13 | ||||
| chr2:17769980-17770101 | Rare:21 | ||||
| chr2:18297682-18298096 | Common:1; Rare:117 | ||||
| chr2:18298129-18298335 | Common:3; Rare:45 | ||||
| chr2:18299486-18299703 | Rare:32 | ||||
| chr2:18307046-18307313 | Rare:50 | ||||
| chr2:18310389-18310427 | Rare:7 | ||||
| chr2:18369900-18370106 | Rare:51 | ||||
| chr2:18507717-18507875 | Rare:42 | ||||
| chr2:18551523-18551818 | Common:2; Rare:51 | ||||
| chr2:19347986-19348102 | Common:1; Rare:49 | ||||
| chr2:19900548-19900732 | Rare:38 | ||||
| chr2:19932368-19932593 | Rare:43; Clinvar:1 |