| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:173965828-173965844 | Rare:5 | ||||
| chr2:173965846-173965889 | Rare:15 | ||||
| chr2:174248463-174248734 | Common:1; Rare:81 | ||||
| chr2:174395629-174395809 | Common:1; Rare:58 | ||||
| chr2:174486961-174487408 | Common:2; Rare:109 | ||||
| chr2:175005172-175005486 | Common:2; Rare:112; Clinvar:2 | ||||
| chr2:176002198-176002414 | Common:4; Rare:89 | ||||
| chr2:176129586-176129730 | Rare:84 | ||||
| chr2:176136747-176136777 | Rare:8 | ||||
| chr2:176188506-176188668 | Common:1; Rare:59 | ||||
| chr2:177212434-177212821 | Common:4; Rare:155 | ||||
| chr2:177231896-177232191 | Common:2; Rare:69 | ||||
| chr2:177263402-177263697 | Common:1; Rare:71 | ||||
| chr2:177264563-177264834 | Common:2; Rare:77 | ||||
| chr2:177392657-177393070 | Common:3; Rare:144; Clinvar:6; Clinvar (benign):4 |