| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:234951805-234952142 | Common:1; Rare:86 | ||||
| chr2:237085706-237085999 | Common:2; Rare:107 | ||||
| chr2:237859065-237859127 | Rare:10 | ||||
| chr2:237859368-237859709 | Common:4; Rare:97 | ||||
| chr2:237966728-237967078 | Common:4; Rare:108 | ||||
| chr2:238060693-238061121 | Common:7; Rare:140 | ||||
| chr2:238203583-238203868 | Common:3; Rare:124 | ||||
| chr2:238426924-238427067 | Common:1; Rare:55 | ||||
| chr2:239401009-239401280 | Common:3; Rare:77 | ||||
| chr2:239401641-239401800 | Rare:84 | ||||
| chr2:240025291-240025529 | Common:2; Rare:104; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr2:240136249-240136439 | Common:1; Rare:84 | ||||
| chr2:240820150-240820463 | Rare:75 | ||||
| chr2:241102269-241102401 | Common:2; Rare:45 | ||||
| chr2:241149434-241149638 | Common:3; Rare:66 |