| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:169694380-169694517 | Common:4; Rare:41 | ||||
| chr2:169798794-169798932 | Rare:40 | ||||
| chr2:171433945-171434267 | Common:2; Rare:83 | ||||
| chr2:171687970-171688040 | Common:1; Rare:12 | ||||
| chr2:171688063-171688299 | Common:1; Rare:54 | ||||
| chr2:174395644-174395795 | Common:1; Rare:52 | ||||
| chr2:175168115-175168511 | Common:2; Rare:104 | ||||
| chr2:177212589-177212816 | Common:1; Rare:95 | ||||
| chr2:177264635-177264802 | Common:2; Rare:54 | ||||
| chr2:177392651-177392795 | Common:1; Rare:35; Clinvar:1 | ||||
| chr2:178451067-178451428 | Common:6; Rare:107; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:186486118-186486364 | Common:3; Rare:84 | ||||
| chr2:187554264-187554547 | Rare:56 | ||||
| chr2:189783953-189784133 | Common:3; Rare:66; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:189784333-189784518 | Common:2; Rare:63; Clinvar:7; Clinvar (benign):1 |