| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:106193607-106194079 | Common:6; Rare:256 | ||||
| chr2:106194217-106194638 | Common:41; Rare:1061 | ||||
| chr2:108377700-108378356 | Common:6; Rare:128 | ||||
| chr2:108448307-108449430 | Common:18; Rare:861 | ||||
| chr2:108533690-108534070 | Common:3; Rare:176 | ||||
| chr2:108534065-108534529 | Common:50; Rare:1014 | ||||
| chr2:108534674-108535074 | Common:4; Rare:113 | ||||
| chr2:108587900-108588651 | Common:10; Rare:324 | ||||
| chr2:108621306-108621706 | Common:2; Rare:171 | ||||
| chr2:108654785-108655185 | Rare:151 | ||||
| chr2:108719254-108719601 | Common:19; Rare:731; Clinvar (benign):8 | ||||
| chr2:108719577-108719977 | Common:2; Rare:149; Clinvar (benign):1 | ||||
| chr2:108786195-108786596 | Common:4; Rare:165 | ||||
| chr2:108786582-108786877 | Common:19; Rare:439 | ||||
| chr2:108786925-108787450 | Common:1; Rare:244 |