| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:219460774-219460957 | Common:1; Rare:37 | ||||
| chr2:219498663-219498995 | Common:2; Rare:76 | ||||
| chr2:219499169-219499255 | Common:2; Rare:12; Clinvar (benign):1 | ||||
| chr2:219542840-219543141 | Common:3; Rare:58 | ||||
| chr2:219543797-219544087 | Common:3; Rare:92 | ||||
| chr2:219598089-219598249 | Rare:44 | ||||
| chr2:221572258-221572576 | Common:6; Rare:115 | ||||
| chr2:222656016-222656478 | Common:3; Rare:153 | ||||
| chr2:222861541-222861726 | Common:1; Rare:48 | ||||
| chr2:223051970-223052321 | Rare:68 | ||||
| chr2:223945152-223945263 | Rare:30 | ||||
| chr2:224039271-224039383 | Rare:42 | ||||
| chr2:224532879-224532922 | Rare:8 | ||||
| chr2:224886206-224886368 | Rare:36 | ||||
| chr2:225042255-225042463 | Common:1; Rare:77 |