| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74465350-74465433 | Rare:24; Clinvar:1 | ||||
| chr2:74503358-74503475 | Rare:27 | ||||
| chr2:74529645-74530036 | Rare:122; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:74833930-74834139 | Rare:62 | ||||
| chr2:74958831-74959071 | Rare:88 | ||||
| chr2:84905457-84905666 | Common:2; Rare:67 | ||||
| chr2:85354531-85354776 | Common:1; Rare:78 | ||||
| chr2:85561443-85561553 | Rare:42; Clinvar:4 | ||||
| chr2:85595558-85595772 | Common:1; Rare:70 | ||||
| chr2:85602662-85602870 | Rare:51 | ||||
| chr2:85612027-85612147 | Rare:29 | ||||
| chr2:96208305-96208415 | Rare:53 | ||||
| chr2:96208817-96208836 | Rare:9 | ||||
| chr2:96265958-96266300 | Common:2; Rare:101; Clinvar:1 | ||||
| chr2:96816153-96816273 | Common:1; Rare:41 |