| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:157257528-157257780 | Rare:51 | ||||
| chr2:157257857-157258078 | Common:1; Rare:37 | ||||
| chr2:158968485-158968702 | Rare:70 | ||||
| chr2:159615429-159615671 | Common:2; Rare:78 | ||||
| chr2:159616437-159616681 | Common:2; Rare:45 | ||||
| chr2:159712375-159712603 | Common:2; Rare:90 | ||||
| chr2:160493805-160494054 | Common:1; Rare:59 | ||||
| chr2:161308351-161308575 | Common:2; Rare:54 | ||||
| chr2:162244836-162244936 | Rare:24 | ||||
| chr2:163736001-163736113 | Rare:22 | ||||
| chr2:164841798-164841951 | Common:1; Rare:44 | ||||
| chr2:165794113-165794309 | Common:2; Rare:54; Clinvar:6; Clinvar (benign):1 | ||||
| chr2:169584303-169584622 | Common:1; Rare:122 | ||||
| chr2:169584703-169584816 | Rare:30 | ||||
| chr2:169694376-169694500 | Common:3; Rare:36 |