| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:73780038-73780224 | Common:1; Rare:84 | ||||
| chr2:73828781-73829054 | Common:2; Rare:66 | ||||
| chr2:73926689-73926956 | Common:2; Rare:127; Clinvar:7; Clinvar (benign):3 | ||||
| chr2:74002480-74002770 | Common:2; Rare:98 | ||||
| chr2:74147872-74148115 | Common:1; Rare:62; Clinvar:2 | ||||
| chr2:74148204-74148906 | Common:7; Rare:225 | ||||
| chr2:74178080-74178504 | Rare:119 | ||||
| chr2:74178808-74179093 | Common:4; Rare:94 | ||||
| chr2:74198358-74198629 | Rare:92 | ||||
| chr2:74199100-74199318 | Rare:48 | ||||
| chr2:74365018-74365418 | Rare:116; Clinvar:4; Clinvar (benign):4 | ||||
| chr2:74374640-74374796 | Rare:29 | ||||
| chr2:74391270-74391670 | Common:6; Rare:121 | ||||
| chr2:74391700-74391950 | Common:1; Rare:130 | ||||
| chr2:74391970-74392240 | Common:2; Rare:85 |