| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:73284777-73284863 | Rare:15 | ||||
| chr2:73737286-73737589 | Common:3; Rare:100 | ||||
| chr2:73828804-73829023 | Common:1; Rare:51 | ||||
| chr2:73926686-73926932 | Common:2; Rare:116; Clinvar:7; Clinvar (benign):3 | ||||
| chr2:73986301-73986431 | Rare:17 | ||||
| chr2:74147821-74148017 | Common:1; Rare:59; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:74369206-74369367 | Rare:52; Clinvar:1 | ||||
| chr2:74421511-74421788 | Rare:88 | ||||
| chr2:74424952-74425231 | Common:3; Rare:87 | ||||
| chr2:74454764-74455119 | Rare:83 | ||||
| chr2:74507644-74507875 | Common:1; Rare:67 | ||||
| chr2:74529656-74529799 | Rare:58; Clinvar:1 | ||||
| chr2:74529801-74530041 | Rare:58; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:74554639-74554777 | Common:1; Rare:62 | ||||
| chr2:74833915-74834147 | Rare:67 |