| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:73986311-73986383 | Rare:9 | ||||
| chr2:74147855-74148062 | Common:1; Rare:59; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:74178763-74179012 | Common:2; Rare:64 | ||||
| chr2:74198512-74198631 | Rare:55 | ||||
| chr2:74362690-74362954 | Common:2; Rare:68; Clinvar:5 | ||||
| chr2:74421600-74421759 | Rare:54 | ||||
| chr2:74440528-74440810 | Rare:72 | ||||
| chr2:74441710-74441783 | Rare:21 | ||||
| chr2:74441820-74442063 | Common:2; Rare:60 | ||||
| chr2:74457888-74458188 | Rare:81 | ||||
| chr2:74459633-74459966 | Rare:113 | ||||
| chr2:74465346-74465459 | Common:1; Rare:31; Clinvar:1 | ||||
| chr2:74482937-74483112 | Common:1; Rare:65 | ||||
| chr2:74507313-74507459 | Rare:45 | ||||
| chr2:74507654-74507824 | Rare:36 |