| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74529607-74530009 | Rare:133; Clinvar:4; Clinvar (benign):1 | ||||
| chr2:74530281-74530593 | Common:4; Rare:103; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:74553941-74554086 | Rare:23 | ||||
| chr2:74554576-74554781 | Common:1; Rare:85 | ||||
| chr2:74554840-74555165 | Rare:88 | ||||
| chr2:74555624-74555798 | Common:1; Rare:50 | ||||
| chr2:74654103-74654285 | Common:1; Rare:46 | ||||
| chr2:74835132-74835310 | Rare:45 | ||||
| chr2:74958530-74958742 | Common:5; Rare:87 | ||||
| chr2:74958876-74959076 | Rare:71 | ||||
| chr2:75710623-75710778 | Common:2; Rare:61 | ||||
| chr2:75710864-75711130 | Common:2; Rare:81 | ||||
| chr2:84459210-84459581 | Common:3; Rare:95; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:84905439-84905953 | Common:2; Rare:155 | ||||
| chr2:84906997-84907349 | Common:1; Rare:65 |