| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:178072688-178072969 | Common:1; Rare:67 | ||||
| chr2:178450731-178450889 | Rare:54 | ||||
| chr2:178451090-178451378 | Common:6; Rare:85; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:178478512-178478659 | Common:1; Rare:46 | ||||
| chr2:180980234-180980545 | Common:1; Rare:95 | ||||
| chr2:181457230-181457669 | Common:2; Rare:164 | ||||
| chr2:181457829-181458325 | Common:2; Rare:142 | ||||
| chr2:181891630-181892037 | Common:4; Rare:171 | ||||
| chr2:182715930-182716440 | Common:3; Rare:167 | ||||
| chr2:183078685-183078792 | Rare:19 | ||||
| chr2:183124284-183124470 | Rare:67 | ||||
| chr2:186485977-186486417 | Common:3; Rare:127 | ||||
| chr2:187553797-187554149 | Rare:62 | ||||
| chr2:187554237-187554514 | Rare:59 | ||||
| chr2:188291607-188291830 | Common:3; Rare:46 |