| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:88628060-88628221 | Rare:28 | ||||
| chr2:88691450-88691853 | Common:2; Rare:158; Clinvar:1 | ||||
| chr2:94588239-94588407 | Rare:38 | ||||
| chr2:95159558-95159828 | Common:4; Rare:83 | ||||
| chr2:95165397-95165464 | Rare:8 | ||||
| chr2:95165651-95165820 | Rare:49 | ||||
| chr2:95207445-95207590 | Rare:59 | ||||
| chr2:95402583-95402761 | Rare:59 | ||||
| chr2:96145438-96145639 | Common:2; Rare:46 | ||||
| chr2:96208225-96208447 | Rare:114 | ||||
| chr2:96208797-96208954 | Common:3; Rare:62 | ||||
| chr2:96265946-96266451 | Common:2; Rare:145; Clinvar:2 | ||||
| chr2:96305414-96305662 | Common:2; Rare:94; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:96536561-96536798 | Common:1; Rare:67 | ||||
| chr2:96638292-96638400 | Rare:32 |