| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:45650975-45651351 | Common:5; Rare:204 | ||||
| chr2:46297040-46297444 | Common:12; Rare:263; Clinvar (benign):1 | ||||
| chr2:46297460-46297908 | Common:2; Rare:179; Clinvar:8; Clinvar (benign):4 | ||||
| chr2:46542272-46542432 | Common:2; Rare:62 | ||||
| chr2:46542555-46542746 | Rare:129 | ||||
| chr2:46616941-46617265 | Common:16; Rare:272 | ||||
| chr2:46698720-46699020 | Common:2; Rare:151 | ||||
| chr2:46699067-46699347 | Common:1; Rare:83 | ||||
| chr2:46915718-46916189 | Common:4; Rare:152; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46940931-46941550 | Common:7; Rare:310 | ||||
| chr2:46941700-46941806 | Common:2; Rare:39; Clinvar (benign):1 | ||||
| chr2:47033910-47034290 | Common:1; Rare:92 | ||||
| chr2:47034370-47034802 | Common:9; Rare:165 | ||||
| chr2:47176020-47177040 | Common:17; Rare:650; Clinvar (benign):10 | ||||
| chr2:47344956-47345325 | Common:4; Rare:185 |