| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:178451126-178451297 | Common:4; Rare:51; Clinvar:3; Clinvar (benign):3 | ||||
| chr2:183124288-183124452 | Rare:58 | ||||
| chr2:186486130-186486344 | Common:3; Rare:71 | ||||
| chr2:189783965-189784072 | Common:2; Rare:34 | ||||
| chr2:189784305-189784506 | Common:3; Rare:65; Clinvar:6; Clinvar (benign):1 | ||||
| chr2:191014133-191014333 | Common:1; Rare:64; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:191677858-191678140 | Common:4; Rare:78 | ||||
| chr2:195656849-195657245 | Common:2; Rare:111 | ||||
| chr2:197434980-197435176 | Rare:66 | ||||
| chr2:197499803-197500430 | Common:1; Rare:239; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:197515873-197516098 | Common:1; Rare:88 | ||||
| chr2:199911024-199911328 | Common:1; Rare:83 | ||||
| chr2:200306432-200306574 | Common:2; Rare:34 | ||||
| chr2:200811272-200811589 | Common:1; Rare:97 | ||||
| chr2:200864635-200864768 | Rare:50 |