| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:159712390-159712593 | Common:2; Rare:83 | ||||
| chr2:162073986-162074014 | Rare:11 | ||||
| chr2:169584569-169584593 | Rare:6 | ||||
| chr2:169584764-169584809 | Rare:14 | ||||
| chr2:171433991-171434225 | Common:1; Rare:63 | ||||
| chr2:171522291-171522525 | Common:3; Rare:54 | ||||
| chr2:171999837-171999964 | Common:1; Rare:55 | ||||
| chr2:174248466-174248730 | Common:1; Rare:79 | ||||
| chr2:174395606-174395788 | Common:2; Rare:59 | ||||
| chr2:175168122-175168553 | Common:2; Rare:112 | ||||
| chr2:176002241-176002406 | Common:2; Rare:67 | ||||
| chr2:177212447-177212821 | Common:4; Rare:150 | ||||
| chr2:177263402-177263719 | Common:1; Rare:77 | ||||
| chr2:177264651-177264813 | Common:2; Rare:54 | ||||
| chr2:177392659-177393005 | Common:3; Rare:122; Clinvar:6; Clinvar (benign):4 |