| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:178441647-178441876 | Common:2; Rare:56; Clinvar (benign):2 | ||||
| chr2:181014008-181014265 | Common:2; Rare:49 | ||||
| chr2:181876686-181876873 | Rare:26 | ||||
| chr2:181895606-181895626 | Rare:2 | ||||
| chr2:181895926-181896085 | Rare:30 | ||||
| chr2:181919363-181919516 | Rare:52 | ||||
| chr2:182754908-182755055 | Rare:42 | ||||
| chr2:182775097-182775421 | Rare:76 | ||||
| chr2:185159706-185159791 | Rare:11 | ||||
| chr2:185956741-185957033 | Common:2; Rare:45 | ||||
| chr2:186208122-186208425 | Common:1; Rare:54 | ||||
| chr2:186406814-186406885 | Common:8; Rare:17 | ||||
| chr2:186592515-186592576 | Rare:11 | ||||
| chr2:186630841-186631120 | Common:1; Rare:57 | ||||
| chr2:186649806-186649883 | Rare:16 |