| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:231961431-231961756 | Common:1; Rare:84; Clinvar:3 | ||||
| chr2:232550466-232550727 | Rare:103 | ||||
| chr2:232550945-232551128 | Common:1; Rare:38 | ||||
| chr2:234951729-234952164 | Common:3; Rare:123 | ||||
| chr2:237085815-237085984 | Common:1; Rare:69 | ||||
| chr2:237335209-237335385 | Rare:20 | ||||
| chr2:237413942-237414407 | Common:2; Rare:90; Clinvar (benign):3 | ||||
| chr2:237487179-237487287 | Common:1; Rare:32 | ||||
| chr2:237627374-237627670 | Common:2; Rare:102 | ||||
| chr2:238025274-238025284 | Common:1; Rare:1 | ||||
| chr2:238060729-238061124 | Common:6; Rare:126 | ||||
| chr2:238426868-238427071 | Common:1; Rare:76 | ||||
| chr2:239401644-239401764 | Rare:58 | ||||
| chr2:240025225-240025427 | Common:2; Rare:72; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr2:240136232-240136333 | Rare:42 |