| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:219206622-219206936 | Rare:116 | ||||
| chr2:219206952-219207352 | Common:8; Rare:243 | ||||
| chr2:219218900-219219170 | Common:2; Rare:86 | ||||
| chr2:219229547-219229912 | Common:2; Rare:115 | ||||
| chr2:219245368-219245548 | Common:1; Rare:54 | ||||
| chr2:219253813-219254213 | Common:4; Rare:161 | ||||
| chr2:219279201-219279427 | Common:2; Rare:71 | ||||
| chr2:219279710-219280160 | Rare:106; Clinvar:1; Clinvar (benign):3 | ||||
| chr2:219388280-219388690 | Common:1; Rare:77 | ||||
| chr2:219441895-219442062 | Rare:37 | ||||
| chr2:219445683-219446478 | Common:5; Rare:172 | ||||
| chr2:219460430-219460830 | Common:6; Rare:96 | ||||
| chr2:219498430-219498600 | Common:2; Rare:38 | ||||
| chr2:219498666-219498947 | Common:2; Rare:64 | ||||
| chr2:219514242-219514642 | Common:6; Rare:286 |