| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:237966723-237967088 | Common:8; Rare:227 | ||||
| chr2:238060691-238061161 | Common:13; Rare:277 | ||||
| chr2:238107480-238107910 | Common:1; Rare:226 | ||||
| chr2:238203574-238203821 | Common:6; Rare:194 | ||||
| chr2:238239958-238240234 | Common:3; Rare:198 | ||||
| chr2:238288734-238288978 | Rare:190 | ||||
| chr2:238320254-238320577 | Common:2; Rare:109 | ||||
| chr2:238426510-238426782 | Common:5; Rare:69 | ||||
| chr2:238426849-238427091 | Common:2; Rare:175 | ||||
| chr2:239400907-239401241 | Common:6; Rare:181 | ||||
| chr2:239401632-239401769 | Rare:125 | ||||
| chr2:240025284-240025525 | Common:4; Rare:188; Clinvar:8; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr2:240136224-240136445 | Common:2; Rare:188 | ||||
| chr2:240560206-240560410 | Rare:155 | ||||
| chr2:240560729-240560884 | Common:2; Rare:143 |