| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:127885950-127885975 | Rare:3 | ||||
| chr2:130181550-130181783 | Common:3; Rare:102 | ||||
| chr2:130182096-130182399 | Common:2; Rare:115 | ||||
| chr2:130182432-130182558 | Common:1; Rare:50 | ||||
| chr2:130342642-130342930 | Common:5; Rare:90 | ||||
| chr2:131493052-131493095 | Common:1; Rare:11 | ||||
| chr2:134918638-134918860 | Common:1; Rare:93 | ||||
| chr2:135531182-135531486 | Common:1; Rare:55 | ||||
| chr2:148020675-148021098 | Common:2; Rare:98; Clinvar (benign):2 | ||||
| chr2:148021502-148021644 | Rare:29 | ||||
| chr2:162073539-162073593 | Rare:15 | ||||
| chr2:169584744-169584809 | Rare:15 | ||||
| chr2:171433988-171434234 | Common:1; Rare:64 | ||||
| chr2:174395638-174395792 | Common:1; Rare:52 | ||||
| chr2:174847547-174847722 | Rare:39 |