| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74147862-74148115 | Common:1; Rare:70; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:74178794-74179066 | Common:4; Rare:84 | ||||
| chr2:74198445-74198664 | Rare:96 | ||||
| chr2:74391793-74391926 | Common:1; Rare:81 | ||||
| chr2:74421609-74421762 | Rare:50 | ||||
| chr2:74465363-74465439 | Rare:18 | ||||
| chr2:74482904-74483106 | Common:1; Rare:67 | ||||
| chr2:74503307-74503454 | Rare:36 | ||||
| chr2:74507315-74507602 | Rare:84 | ||||
| chr2:74507669-74507781 | Rare:24 | ||||
| chr2:74527470-74527744 | Common:1; Rare:93 | ||||
| chr2:74529654-74530036 | Rare:117; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:74553941-74554171 | Rare:49 | ||||
| chr2:74554656-74554755 | Common:1; Rare:41 | ||||
| chr2:74958872-74959032 | Rare:61 |