| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:216107641-216108164 | Common:6; Rare:159 | ||||
| chr2:216108901-216109601 | Common:49; Rare:688 | ||||
| chr2:216109612-216110048 | Rare:210 | ||||
| chr2:216412174-216412900 | Common:15; Rare:426; Clinvar:6; Clinvar (benign):9 | ||||
| chr2:216497690-216498098 | Common:6; Rare:243 | ||||
| chr2:216498130-216498530 | Common:4; Rare:67 | ||||
| chr2:216498540-216499250 | Common:56; Rare:730 | ||||
| chr2:216862632-216863032 | Common:2; Rare:65 | ||||
| chr2:217842048-217842448 | Common:9; Rare:174 | ||||
| chr2:217858608-217858765 | Common:1; Rare:25 | ||||
| chr2:217901843-217902271 | Common:5; Rare:76 | ||||
| chr2:218216910-218217340 | Common:13; Rare:623 | ||||
| chr2:218217314-218218094 | Common:10; Rare:461 | ||||
| chr2:218269441-218269892 | Rare:318 | ||||
| chr2:218270061-218270565 | Common:35; Rare:1015; Clinvar:22; Clinvar (benign):8 |