| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:71129961-71130829 | Common:35; Rare:931; Clinvar:7; Clinvar (benign):14 | ||||
| chr2:71130865-71131265 | Common:4; Rare:88 | ||||
| chr2:71331463-71331874 | Common:13; Rare:261 | ||||
| chr2:71417463-71418007 | Common:10; Rare:239 | ||||
| chr2:71453300-71453822 | Common:5; Rare:237 | ||||
| chr2:72825890-72826260 | Common:1; Rare:101 | ||||
| chr2:72887059-72887555 | Common:8; Rare:497; Clinvar:1; Clinvar (benign):9 | ||||
| chr2:72887841-72888241 | Common:4; Rare:120 | ||||
| chr2:73070019-73070447 | Common:1; Rare:127 | ||||
| chr2:73070449-73070849 | Common:9; Rare:209 | ||||
| chr2:73070930-73071599 | Common:13; Rare:677 | ||||
| chr2:73071605-73072005 | Common:9; Rare:377 | ||||
| chr2:73112651-73113390 | Common:36; Rare:961 | ||||
| chr2:73214015-73214415 | Common:7; Rare:449 | ||||
| chr2:73214360-73215040 | Common:19; Rare:552 |