| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:191245254-191245562 | Common:2; Rare:99 | ||||
| chr2:191677856-191678173 | Common:4; Rare:91 | ||||
| chr2:195656955-195657273 | Common:2; Rare:81 | ||||
| chr2:196171454-196171833 | Common:1; Rare:108 | ||||
| chr2:196799574-196799779 | Common:1; Rare:68 | ||||
| chr2:196926722-196926788 | Common:1; Rare:24 | ||||
| chr2:197434973-197435192 | Rare:75 | ||||
| chr2:197453222-197453571 | Rare:119 | ||||
| chr2:197499783-197500424 | Common:2; Rare:244; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:197515835-197516095 | Common:2; Rare:94 | ||||
| chr2:197516678-197516791 | Common:1; Rare:43 | ||||
| chr2:200510047-200510221 | Common:1; Rare:50 | ||||
| chr2:200811437-200811610 | Common:1; Rare:63 | ||||
| chr2:200811796-200811964 | Rare:68 | ||||
| chr2:200864137-200864264 | Rare:51 |