| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:37084262-37084570 | Common:4; Rare:115 | ||||
| chr2:37231551-37231710 | Common:4; Rare:92; Clinvar (benign):3 | ||||
| chr2:37344636-37344726 | Common:1; Rare:37 | ||||
| chr2:38377243-38377509 | Common:2; Rare:105 | ||||
| chr2:38602895-38602992 | Common:1; Rare:38 | ||||
| chr2:38751348-38751574 | Common:2; Rare:95 | ||||
| chr2:38875881-38876076 | Common:2; Rare:73 | ||||
| chr2:39437103-39437453 | Common:4; Rare:122 | ||||
| chr2:39665297-39665488 | Rare:41 | ||||
| chr2:44361479-44361585 | Common:1; Rare:35 | ||||
| chr2:44361745-44362002 | Common:1; Rare:79 | ||||
| chr2:46617012-46617261 | Common:6; Rare:108 | ||||
| chr2:46915738-46915908 | Common:1; Rare:51; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:47176440-47176873 | Common:4; Rare:194; Clinvar (benign):5 | ||||
| chr2:47344993-47345190 | Common:1; Rare:53 |