| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:230200889-230201184 | Common:3; Rare:67; Clinvar (benign):1 | ||||
| chr2:230507209-230507436 | Rare:41 | ||||
| chr2:230510765-230510878 | Common:2; Rare:16 | ||||
| chr2:230514943-230515312 | Common:1; Rare:115 | ||||
| chr2:230527301-230527586 | Common:1; Rare:40 | ||||
| chr2:230927736-230927819 | Common:1; Rare:22 | ||||
| chr2:231459035-231459417 | Common:3; Rare:96 | ||||
| chr2:231514357-231514542 | Common:5; Rare:72 | ||||
| chr2:231666432-231666675 | Rare:54 | ||||
| chr2:231712608-231713016 | Common:5; Rare:136 | ||||
| chr2:232791011-232791324 | Rare:93 | ||||
| chr2:233079121-233079505 | Common:1; Rare:83 | ||||
| chr2:233079724-233079996 | Common:4; Rare:49 | ||||
| chr2:233146413-233146622 | Rare:44 | ||||
| chr2:233180091-233180118 | Rare:4 |