| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:71068093-71068408 | Rare:82 | ||||
| chr2:71068441-71068746 | Rare:137 | ||||
| chr2:71068846-71068937 | Common:1; Rare:16 | ||||
| chr2:71070786-71070971 | Common:1; Rare:44 | ||||
| chr2:71129961-71130693 | Common:7; Rare:202; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:71130786-71131100 | Common:2; Rare:70 | ||||
| chr2:71227084-71227415 | Common:2; Rare:78 | ||||
| chr2:71276420-71276676 | Rare:101 | ||||
| chr2:71276767-71276956 | Common:1; Rare:42 | ||||
| chr2:71331565-71331853 | Common:5; Rare:90 | ||||
| chr2:72887233-72887448 | Common:1; Rare:71; Clinvar (benign):1 | ||||
| chr2:72916225-72916424 | Common:1; Rare:53 | ||||
| chr2:72916467-72916615 | Rare:31 | ||||
| chr2:72917153-72917192 | Rare:6 | ||||
| chr2:72917237-72917627 | Common:6; Rare:111 |