| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:219178800-219179347 | Rare:238 | ||||
| chr2:219206574-219206946 | Rare:304 | ||||
| chr2:219206889-219207075 | Rare:64 | ||||
| chr2:219216191-219216452 | Rare:87 | ||||
| chr2:219217762-219218211 | Common:3; Rare:160; Clinvar:2 | ||||
| chr2:219229272-219229430 | Rare:77 | ||||
| chr2:219229501-219229964 | Common:7; Rare:387 | ||||
| chr2:219245329-219245624 | Common:4; Rare:176 | ||||
| chr2:219253862-219254156 | Common:4; Rare:183 | ||||
| chr2:219279176-219279564 | Common:6; Rare:208; Clinvar (benign):2 | ||||
| chr2:219387306-219387585 | Common:3; Rare:114 | ||||
| chr2:219387651-219388237 | Common:5; Rare:345 | ||||
| chr2:219388220-219388728 | Common:2; Rare:161 | ||||
| chr2:219399956-219400500 | Common:3; Rare:155 | ||||
| chr2:219441760-219442250 | Rare:191 |