| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:73385689-73386023 | Common:4; Rare:157; Clinvar:16; Clinvar (benign):8 | ||||
| chr2:73828804-73829024 | Common:1; Rare:51 | ||||
| chr2:74147874-74148051 | Common:1; Rare:44; Clinvar:2 | ||||
| chr2:74178812-74179009 | Common:2; Rare:55 | ||||
| chr2:74421571-74421771 | Rare:67 | ||||
| chr2:74458146-74458498 | Common:1; Rare:106 | ||||
| chr2:74482937-74483098 | Common:1; Rare:57 | ||||
| chr2:74529669-74529997 | Rare:95; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:74958488-74958672 | Common:2; Rare:63 | ||||
| chr2:74958876-74959003 | Rare:51 | ||||
| chr2:84459213-84459572 | Common:3; Rare:92; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:84905512-84905859 | Common:1; Rare:109 | ||||
| chr2:85327927-85328080 | Common:2; Rare:71 | ||||
| chr2:85354517-85354786 | Common:1; Rare:88 | ||||
| chr2:85539057-85539179 | Common:2; Rare:48 |