| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74147855-74148149 | Common:1; Rare:77; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:74178779-74179066 | Common:4; Rare:85 | ||||
| chr2:74421609-74421764 | Rare:52 | ||||
| chr2:74458100-74458655 | Common:2; Rare:177 | ||||
| chr2:74459518-74459936 | Rare:122 | ||||
| chr2:74465339-74465445 | Rare:28; Clinvar:1 | ||||
| chr2:74472360-74472750 | Common:4; Rare:178 | ||||
| chr2:74482916-74483106 | Common:1; Rare:64 | ||||
| chr2:74503031-74503165 | Rare:27 | ||||
| chr2:74503300-74503445 | Rare:38 | ||||
| chr2:74507635-74507789 | Rare:38 | ||||
| chr2:74527470-74527743 | Common:1; Rare:92 | ||||
| chr2:74529606-74530036 | Rare:141; Clinvar:4; Clinvar (benign):1 | ||||
| chr2:74530539-74530624 | Common:1; Rare:33; Clinvar:2 | ||||
| chr2:74554687-74554755 | Common:1; Rare:32 |