| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:95818150-95818283 | Rare:19 | ||||
| chr2:95818324-95818352 | Rare:3 | ||||
| chr2:95819080-95819223 | Rare:23 | ||||
| chr2:95820337-95820611 | Rare:49 | ||||
| chr2:95825467-95825517 | Rare:10 | ||||
| chr2:95827345-95827390 | Rare:4 | ||||
| chr2:95827786-95828051 | Rare:36 | ||||
| chr2:95915994-95916153 | Rare:70 | ||||
| chr2:96201439-96201574 | Rare:24 | ||||
| chr2:96276973-96277254 | Common:1; Rare:84; Clinvar:4; Clinvar (benign):2 | ||||
| chr2:96329583-96329888 | Rare:52 | ||||
| chr2:96345515-96345887 | Common:1; Rare:58 | ||||
| chr2:96377077-96377191 | Rare:18 | ||||
| chr2:96481674-96481822 | Rare:24 | ||||
| chr2:96538670-96538919 | Rare:43 |