| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:178478515-178478637 | Common:1; Rare:40 | ||||
| chr2:179264508-179264857 | Common:4; Rare:130 | ||||
| chr2:182426616-182426890 | Common:1; Rare:52 | ||||
| chr2:182716161-182716380 | Common:2; Rare:73 | ||||
| chr2:186486118-186486344 | Common:3; Rare:73 | ||||
| chr2:188974360-188974564 | Rare:59; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr2:189441078-189441407 | Common:1; Rare:82 | ||||
| chr2:189783965-189784093 | Common:3; Rare:45; Clinvar (benign):1 | ||||
| chr2:189784305-189784506 | Common:3; Rare:65; Clinvar:6; Clinvar (benign):1 | ||||
| chr2:191014143-191014381 | Common:2; Rare:89; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:191677854-191678201 | Common:4; Rare:98 | ||||
| chr2:197434973-197435198 | Rare:76 | ||||
| chr2:197499815-197500196 | Rare:138; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:197500219-197500430 | Common:1; Rare:86 | ||||
| chr2:200509929-200510192 | Common:1; Rare:90 |