| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:71068889-71069124 | Rare:45 | ||||
| chr2:71129911-71130027 | Rare:22 | ||||
| chr2:71130141-71130390 | Common:3; Rare:89; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:71130428-71130825 | Common:4; Rare:121 | ||||
| chr2:71131030-71131126 | Common:1; Rare:20 | ||||
| chr2:71227002-71227418 | Common:2; Rare:102 | ||||
| chr2:71276450-71276631 | Rare:65 | ||||
| chr2:71276796-71277083 | Common:1; Rare:59 | ||||
| chr2:71331563-71331900 | Common:5; Rare:103 | ||||
| chr2:71331950-71332051 | Common:2; Rare:26 | ||||
| chr2:71332178-71332291 | Rare:32 | ||||
| chr2:72515395-72516076 | Common:3; Rare:115 | ||||
| chr2:72825861-72826163 | Rare:96 | ||||
| chr2:72887567-72887582 | Rare:3 | ||||
| chr2:73070542-73070607 | Common:1; Rare:11 |