| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:42169148-42169468 | Common:1; Rare:149 | ||||
| chr2:43595904-43596222 | Common:1; Rare:111 | ||||
| chr2:43637094-43637379 | Common:2; Rare:94 | ||||
| chr2:43676383-43676676 | Common:2; Rare:79 | ||||
| chr2:43995959-43996344 | Common:4; Rare:162; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:44361479-44362032 | Common:4; Rare:175 | ||||
| chr2:46297159-46297409 | Common:4; Rare:98 | ||||
| chr2:46543040-46543188 | Rare:40 | ||||
| chr2:46543458-46543783 | Common:1; Rare:88 | ||||
| chr2:46616977-46617281 | Common:7; Rare:129 | ||||
| chr2:46698749-46698940 | Common:1; Rare:56 | ||||
| chr2:46915722-46915935 | Common:2; Rare:70; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46916007-46916128 | Common:2; Rare:36 | ||||
| chr2:46941710-46941787 | Common:1; Rare:30; Clinvar (benign):1 | ||||
| chr2:47176434-47176925 | Common:5; Rare:223; Clinvar (benign):5 |