| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:197489147-197489447 | Common:1; Rare:71; Clinvar (benign):1 | ||||
| chr2:197548231-197548352 | Rare:23 | ||||
| chr2:199933295-199933616 | Rare:64 | ||||
| chr2:200412118-200412419 | Common:1; Rare:52 | ||||
| chr2:201017128-201017250 | Rare:35 | ||||
| chr2:201278005-201278284 | Common:2; Rare:37 | ||||
| chr2:201278550-201278880 | Common:1; Rare:56 | ||||
| chr2:202036226-202036423 | Rare:68 | ||||
| chr2:202037247-202037554 | Rare:50 | ||||
| chr2:202376071-202376360 | Rare:122 | ||||
| chr2:203448057-203448178 | Rare:25 | ||||
| chr2:203448780-203448958 | Rare:32 | ||||
| chr2:203461866-203462084 | Rare:36 | ||||
| chr2:205765416-205765501 | Rare:26 | ||||
| chr2:206084358-206084658 | Common:1; Rare:63 |