| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:134918632-134918857 | Common:1; Rare:93 | ||||
| chr2:135531172-135531514 | Common:1; Rare:72 | ||||
| chr2:148020673-148021005 | Common:2; Rare:72 | ||||
| chr2:149587702-149587883 | Common:1; Rare:51; Clinvar:1 | ||||
| chr2:152718481-152718637 | Rare:61 | ||||
| chr2:156332714-156332870 | Rare:48; Clinvar:2 | ||||
| chr2:159712411-159712544 | Common:2; Rare:58 | ||||
| chr2:159904693-159904848 | Rare:41 | ||||
| chr2:161308334-161308537 | Common:2; Rare:53 | ||||
| chr2:165794187-165794358 | Common:2; Rare:48; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:169694360-169694487 | Common:2; Rare:40 | ||||
| chr2:171433955-171434224 | Common:2; Rare:71 | ||||
| chr2:173354586-173354901 | Common:1; Rare:94 | ||||
| chr2:174248454-174248730 | Common:1; Rare:83 | ||||
| chr2:175181647-175181736 | Common:3; Rare:45 |