| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:165794087-165794538 | Common:4; Rare:112; Clinvar:6; Clinvar (benign):1 | ||||
| chr2:165794630-165794780 | Common:1; Rare:25 | ||||
| chr2:169584759-169584804 | Rare:12 | ||||
| chr2:169694376-169694517 | Common:4; Rare:42 | ||||
| chr2:171433960-171434248 | Common:2; Rare:70 | ||||
| chr2:171522291-171522480 | Common:3; Rare:42 | ||||
| chr2:171894217-171894364 | Rare:62; Clinvar:1 | ||||
| chr2:171922190-171922497 | Rare:112 | ||||
| chr2:171999837-171999972 | Common:1; Rare:55 | ||||
| chr2:173354608-173354935 | Common:1; Rare:103 | ||||
| chr2:174248460-174248758 | Common:1; Rare:92 | ||||
| chr2:174395628-174395794 | Common:1; Rare:55 | ||||
| chr2:175181647-175181762 | Common:3; Rare:49 | ||||
| chr2:176002242-176002407 | Common:2; Rare:68 | ||||
| chr2:176104087-176104535 | Common:2; Rare:103 |