| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:42493981-42494174 | Rare:84 | ||||
| chr2:42792514-42792757 | Common:2; Rare:76 | ||||
| chr2:43225721-43226021 | Common:3; Rare:122 | ||||
| chr2:43226232-43226443 | Common:1; Rare:88 | ||||
| chr2:43226517-43226875 | Common:3; Rare:150 | ||||
| chr2:43595957-43596205 | Common:1; Rare:90 | ||||
| chr2:43995959-43996302 | Common:4; Rare:146; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:44322832-44322981 | Rare:43; Clinvar:1 | ||||
| chr2:44361469-44362010 | Common:4; Rare:171 | ||||
| chr2:46297153-46297431 | Common:4; Rare:108 | ||||
| chr2:46616978-46617270 | Common:7; Rare:129 | ||||
| chr2:46698944-46699323 | Common:1; Rare:119 | ||||
| chr2:46915722-46915908 | Common:1; Rare:56; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46916033-46916167 | Common:2; Rare:45 | ||||
| chr2:46941694-46941787 | Common:2; Rare:37; Clinvar (benign):1 |