| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:201116576-201117271 | Rare:218 | ||||
| chr2:201257850-201258100 | Common:1; Rare:44 | ||||
| chr2:201357320-201357545 | Rare:43 | ||||
| chr2:201450997-201451108 | Common:1; Rare:23 | ||||
| chr2:201451390-201451980 | Common:3; Rare:142 | ||||
| chr2:201642384-201642815 | Common:4; Rare:140; Clinvar (benign):1 | ||||
| chr2:201643370-201643750 | Common:3; Rare:89; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:201780300-201780700 | Common:2; Rare:140 | ||||
| chr2:201780887-201781260 | Common:3; Rare:118; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:202238513-202238724 | Common:1; Rare:71 | ||||
| chr2:202265618-202265799 | Rare:64 | ||||
| chr2:202376968-202377573 | Common:4; Rare:222; Clinvar:3; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr2:202634658-202635024 | Common:6; Rare:121 | ||||
| chr2:202635856-202636068 | Common:5; Rare:65 | ||||
| chr2:202871431-202871586 | Common:3; Rare:53 |