| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:159615090-159615793 | Common:39; Rare:1194 | ||||
| chr2:159615730-159616160 | Common:2; Rare:183 | ||||
| chr2:159616395-159616790 | Common:4; Rare:117 | ||||
| chr2:159617077-159617477 | Common:2; Rare:65 | ||||
| chr2:159711766-159712630 | Common:32; Rare:1153 | ||||
| chr2:159712690-159713178 | Common:3; Rare:189 | ||||
| chr2:161136658-161137058 | Common:1; Rare:115 | ||||
| chr2:161160080-161161193 | Common:14; Rare:844 | ||||
| chr2:161307853-161308162 | Common:1; Rare:101 | ||||
| chr2:161308150-161308897 | Common:13; Rare:708 | ||||
| chr2:162318541-162319033 | Common:3; Rare:318 | ||||
| chr2:164840671-164841823 | Common:2; Rare:776 | ||||
| chr2:165953208-165953608 | Common:3; Rare:79 | ||||
| chr2:165953665-165954065 | Common:9; Rare:517; Clinvar:41; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr2:165954088-165954370 | Common:5; Rare:169 |