| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:230416101-230416312 | Rare:66 | ||||
| chr2:231460275-231460562 | Common:1; Rare:110 | ||||
| chr2:231708495-231708568 | Rare:32 | ||||
| chr2:231710268-231710570 | Common:2; Rare:147 | ||||
| chr2:231961663-231961742 | Rare:20; Clinvar:1 | ||||
| chr2:232550514-232550721 | Rare:85 | ||||
| chr2:232550970-232551090 | Common:1; Rare:24 | ||||
| chr2:237085819-237085941 | Common:1; Rare:44 | ||||
| chr2:238060761-238061052 | Common:4; Rare:92 | ||||
| chr2:240025229-240025476 | Common:2; Rare:90; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr2:240560760-240560816 | Rare:21 | ||||
| chr2:240561007-240561315 | Common:4; Rare:147 | ||||
| chr2:240625032-240625250 | Rare:52 | ||||
| chr2:240625253-240625572 | Common:1; Rare:66 | ||||
| chr2:240625654-240625884 | Common:10; Rare:27 |