| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:73829334-73829471 | Common:4; Rare:28 | ||||
| chr2:73926733-73926950 | Common:2; Rare:114; Clinvar:7; Clinvar (benign):3 | ||||
| chr2:74147821-74148037 | Common:1; Rare:63; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:74178668-74178732 | Rare:13 | ||||
| chr2:74178751-74178927 | Common:1; Rare:44 | ||||
| chr2:74198380-74198629 | Rare:86 | ||||
| chr2:74362651-74363032 | Common:3; Rare:109; Clinvar:5; Clinvar (benign):7 | ||||
| chr2:74421558-74421779 | Rare:71 | ||||
| chr2:74440413-74440634 | Rare:57 | ||||
| chr2:74458372-74458522 | Rare:48 | ||||
| chr2:74465350-74465445 | Rare:26; Clinvar:1 | ||||
| chr2:74482996-74483113 | Rare:48 | ||||
| chr2:74502477-74502599 | Rare:31 | ||||
| chr2:74503044-74503161 | Rare:26 | ||||
| chr2:74503345-74503425 | Rare:17 |