| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:61538964-61539093 | Rare:33 | ||||
| chr2:61853949-61854192 | Common:2; Rare:103; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:61854516-61854731 | Rare:41 | ||||
| chr2:61888309-61888776 | Common:2; Rare:205 | ||||
| chr2:61905568-61905708 | Rare:57 | ||||
| chr2:62506130-62506353 | Common:1; Rare:87 | ||||
| chr2:62705579-62705907 | Rare:71 | ||||
| chr2:63050589-63050815 | Common:1; Rare:60 | ||||
| chr2:63588220-63589046 | Common:2; Rare:259; Clinvar:6; Clinvar (benign):1 | ||||
| chr2:63840791-63841167 | Common:2; Rare:111 | ||||
| chr2:63841684-63841898 | Common:1; Rare:75 | ||||
| chr2:64144319-64144547 | Common:4; Rare:67 | ||||
| chr2:64524073-64524467 | Common:3; Rare:129 | ||||
| chr2:64653768-64654077 | Common:1; Rare:111 | ||||
| chr2:64989058-64989421 | Common:7; Rare:96 |