| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:189784276-189784518 | Common:4; Rare:82; Clinvar:8; Clinvar (benign):2 | ||||
| chr2:190343864-190343938 | Rare:13 | ||||
| chr2:190343961-190344025 | Rare:12 | ||||
| chr2:190534659-190534862 | Common:1; Rare:65 | ||||
| chr2:190648728-190649119 | Common:2; Rare:133 | ||||
| chr2:191014122-191014415 | Common:3; Rare:106; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:191677856-191678181 | Common:4; Rare:94 | ||||
| chr2:191846745-191846812 | Rare:18 | ||||
| chr2:197434973-197435181 | Rare:71 | ||||
| chr2:197453180-197453569 | Rare:134 | ||||
| chr2:197499815-197500427 | Common:1; Rare:237; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:197515883-197516087 | Common:1; Rare:80 | ||||
| chr2:200509907-200510263 | Common:2; Rare:121 | ||||
| chr2:200609159-200609359 | Rare:50 | ||||
| chr2:200811324-200811580 | Common:1; Rare:79 |