| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:205682212-205682516 | Rare:70 | ||||
| chr2:206085772-206085969 | Common:1; Rare:56 | ||||
| chr2:206086272-206086303 | Rare:3 | ||||
| chr2:206159192-206160058 | Common:6; Rare:250; Clinvar (benign):2 | ||||
| chr2:206274955-206275071 | Common:1; Rare:42 | ||||
| chr2:206765276-206765652 | Common:3; Rare:104; Clinvar:4; Clinvar (benign):5 | ||||
| chr2:207165928-207166122 | Rare:34 | ||||
| chr2:207529768-207530116 | Common:3; Rare:95 | ||||
| chr2:207625176-207625591 | Common:1; Rare:116 | ||||
| chr2:208254384-208254502 | Rare:31 | ||||
| chr2:208254995-208255238 | Common:2; Rare:62 | ||||
| chr2:209424147-209424258 | Common:2; Rare:29 | ||||
| chr2:209579373-209579735 | Common:1; Rare:67 | ||||
| chr2:209661355-209661573 | Common:2; Rare:35 | ||||
| chr2:209771709-209772075 | Common:2; Rare:103 |