| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:158968516-158968646 | Rare:39 | ||||
| chr2:159712409-159712593 | Common:2; Rare:74 | ||||
| chr2:161308325-161308537 | Common:2; Rare:56 | ||||
| chr2:171160343-171160382 | Rare:14 | ||||
| chr2:171433940-171434234 | Common:3; Rare:77 | ||||
| chr2:171894221-171894364 | Rare:61; Clinvar:1 | ||||
| chr2:171922289-171922497 | Rare:80 | ||||
| chr2:171999806-171999961 | Common:1; Rare:68 | ||||
| chr2:173354543-173354912 | Common:1; Rare:112 | ||||
| chr2:174248460-174248779 | Common:1; Rare:103 | ||||
| chr2:174395678-174395736 | Common:1; Rare:19 | ||||
| chr2:175181629-175181843 | Common:4; Rare:75 | ||||
| chr2:177212434-177212797 | Common:4; Rare:148 | ||||
| chr2:177392672-177392829 | Rare:45; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:177552768-177552829 | Rare:22 |