| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:38075932-38075978 | Common:1; Rare:12 | ||||
| chr2:38076043-38076291 | Common:1; Rare:64 | ||||
| chr2:38602863-38603163 | Common:4; Rare:122 | ||||
| chr2:38751292-38751628 | Common:6; Rare:173 | ||||
| chr2:38875886-38876059 | Common:1; Rare:63 | ||||
| chr2:39437078-39437456 | Common:4; Rare:136 | ||||
| chr2:43226311-43226351 | Rare:17 | ||||
| chr2:43226538-43226811 | Common:2; Rare:111 | ||||
| chr2:43595957-43596203 | Common:1; Rare:89 | ||||
| chr2:44361484-44362005 | Common:3; Rare:164 | ||||
| chr2:46617019-46617261 | Common:6; Rare:105 | ||||
| chr2:46915724-46915908 | Common:1; Rare:55; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:48440631-48440956 | Common:7; Rare:146 | ||||
| chr2:51032095-51032374 | Rare:86; Clinvar:7 | ||||
| chr2:53767559-53767866 | Common:4; Rare:106 |