| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:206274839-206275057 | Common:1; Rare:67 | ||||
| chr2:206765273-206765662 | Common:3; Rare:109; Clinvar:4; Clinvar (benign):5 | ||||
| chr2:207165928-207166120 | Rare:34 | ||||
| chr2:207529768-207530108 | Common:3; Rare:95 | ||||
| chr2:208190000-208190070 | Rare:22 | ||||
| chr2:208254395-208254507 | Rare:28 | ||||
| chr2:208255003-208255238 | Common:2; Rare:61 | ||||
| chr2:208266119-208266355 | Common:6; Rare:85; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:209424161-209424230 | Rare:17 | ||||
| chr2:209579254-209579566 | Common:8; Rare:60 | ||||
| chr2:209579569-209579731 | Common:1; Rare:26 | ||||
| chr2:209771778-209772039 | Common:1; Rare:72 | ||||
| chr2:210002287-210002670 | Common:6; Rare:111 | ||||
| chr2:210170686-210170896 | Common:1; Rare:81 | ||||
| chr2:210476653-210476820 | Rare:61 |