| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:156435481-156435800 | Common:1; Rare:73 | ||||
| chr2:156436273-156436511 | Common:3; Rare:68 | ||||
| chr2:158456713-158456973 | Common:1; Rare:92 | ||||
| chr2:158968516-158968747 | Rare:71 | ||||
| chr2:159614991-159615343 | Common:3; Rare:68 | ||||
| chr2:159615428-159615696 | Common:2; Rare:86 | ||||
| chr2:159616411-159616531 | Common:1; Rare:29 | ||||
| chr2:159712345-159712651 | Common:2; Rare:107 | ||||
| chr2:160407877-160408146 | Common:1; Rare:74 | ||||
| chr2:161308334-161308595 | Common:2; Rare:63 | ||||
| chr2:162318656-162318804 | Rare:29 | ||||
| chr2:163735995-163735998 | |||||
| chr2:163736001-163736102 | Rare:20 | ||||
| chr2:164621120-164621236 | Rare:27 | ||||
| chr2:165953733-165953987 | Common:2; Rare:99; Clinvar:6; Clinvar (benign):1 |