| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:159712334-159712600 | Common:2; Rare:98 | ||||
| chr2:160062474-160062740 | Common:5; Rare:66 | ||||
| chr2:161160161-161160489 | Common:2; Rare:91 | ||||
| chr2:161160671-161160726 | Rare:14 | ||||
| chr2:161160850-161161163 | Common:1; Rare:68 | ||||
| chr2:161308334-161308750 | Common:2; Rare:92 | ||||
| chr2:162343893-162344196 | Common:1; Rare:97 | ||||
| chr2:163735878-163736121 | Common:1; Rare:37 | ||||
| chr2:164841200-164841561 | Rare:106 | ||||
| chr2:164841873-164841913 | Rare:12 | ||||
| chr2:165953723-165953866 | Common:1; Rare:64; Clinvar:6; Clinvar (benign):2 | ||||
| chr2:166375867-166376072 | Common:3; Rare:56; Clinvar:1; Clinvar (benign):5 | ||||
| chr2:168456481-168456531 | Rare:14 | ||||
| chr2:169479377-169479565 | Common:3; Rare:74; Clinvar (benign):1 | ||||
| chr2:169584303-169584646 | Common:1; Rare:131 |