| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:233854343-233854781 | Common:6; Rare:133 | ||||
| chr2:234951775-234952105 | Common:2; Rare:88 | ||||
| chr2:234981343-234981413 | Common:1; Rare:14 | ||||
| chr2:236167323-236167483 | Common:2; Rare:68 | ||||
| chr2:237085819-237085976 | Common:1; Rare:66 | ||||
| chr2:237486331-237486490 | Rare:34 | ||||
| chr2:237487100-237487323 | Common:3; Rare:61 | ||||
| chr2:237517532-237518329 | Common:19; Rare:129 | ||||
| chr2:237545903-237546040 | Common:1; Rare:28 | ||||
| chr2:237552025-237552307 | Common:6; Rare:42 | ||||
| chr2:238060729-238061138 | Common:6; Rare:130 | ||||
| chr2:238426855-238427061 | Common:1; Rare:76 | ||||
| chr2:239401644-239401760 | Rare:56 | ||||
| chr2:240025225-240025451 | Common:2; Rare:81; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr2:240560735-240560888 | Common:2; Rare:71 |