| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:37324773-37324950 | Common:1; Rare:69 | ||||
| chr2:37671636-37671739 | Common:1; Rare:51 | ||||
| chr2:38602895-38603163 | Common:4; Rare:106 | ||||
| chr2:38751336-38751645 | Common:4; Rare:146 | ||||
| chr2:38875886-38876055 | Common:1; Rare:63 | ||||
| chr2:39437283-39437447 | Common:2; Rare:56 | ||||
| chr2:42169160-42169431 | Common:1; Rare:135 | ||||
| chr2:43595984-43596205 | Common:1; Rare:76 | ||||
| chr2:43637094-43637328 | Common:2; Rare:79 | ||||
| chr2:43996255-43996335 | Rare:26 | ||||
| chr2:44361483-44362059 | Common:4; Rare:187 | ||||
| chr2:44941445-44941748 | Rare:66 | ||||
| chr2:46616986-46617262 | Common:7; Rare:121 | ||||
| chr2:46915733-46915939 | Common:2; Rare:67; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46916021-46916135 | Common:2; Rare:34 |