| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:179264521-179264839 | Common:3; Rare:120 | ||||
| chr2:180007061-180007406 | Common:1; Rare:82 | ||||
| chr2:180980229-180980458 | Common:1; Rare:68 | ||||
| chr2:181457253-181457565 | Common:2; Rare:109 | ||||
| chr2:181891661-181892461 | Common:6; Rare:298 | ||||
| chr2:182715941-182716406 | Common:3; Rare:153 | ||||
| chr2:183078661-183078799 | Rare:29 | ||||
| chr2:183124252-183124484 | Common:4; Rare:79 | ||||
| chr2:186485987-186486455 | Common:3; Rare:136 | ||||
| chr2:188291845-188291945 | Common:1; Rare:39 | ||||
| chr2:188292692-188292893 | Common:1; Rare:48 | ||||
| chr2:189441094-189441511 | Common:2; Rare:127 | ||||
| chr2:189580769-189580938 | Rare:47; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:189783956-189784125 | Common:3; Rare:62; Clinvar (benign):1 | ||||
| chr2:189784276-189784547 | Common:4; Rare:98; Clinvar:8; Clinvar (benign):2 |