| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:216694488-216694853 | Rare:92 | ||||
| chr2:216695519-216695580 | Rare:12 | ||||
| chr2:217813683-217813995 | Common:1; Rare:74 | ||||
| chr2:217901887-217902122 | Common:3; Rare:44 | ||||
| chr2:217903788-217903895 | Common:1; Rare:16 | ||||
| chr2:217978622-217978686 | Rare:20 | ||||
| chr2:217978765-217978941 | Common:1; Rare:51 | ||||
| chr2:217979245-217979359 | Common:3; Rare:17 | ||||
| chr2:218217057-218217246 | Common:1; Rare:67 | ||||
| chr2:218270082-218270538 | Common:5; Rare:144; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:218271263-218271544 | Rare:78; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:218287255-218287427 | Common:1; Rare:29 | ||||
| chr2:218292470-218292707 | Common:1; Rare:65 | ||||
| chr2:218399506-218399668 | Common:1; Rare:65 | ||||
| chr2:218568297-218568688 | Common:4; Rare:98 |