| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:42494892-42495211 | Common:1; Rare:72 | ||||
| chr2:42568499-42568537 | Rare:8 | ||||
| chr2:42568586-42568742 | Common:3; Rare:52 | ||||
| chr2:42569137-42569326 | Common:2; Rare:51 | ||||
| chr2:42569366-42569446 | Rare:9 | ||||
| chr2:42792514-42792816 | Common:3; Rare:91 | ||||
| chr2:43226008-43226151 | Common:1; Rare:52 | ||||
| chr2:43226327-43226942 | Common:5; Rare:255 | ||||
| chr2:43226985-43227482 | Common:2; Rare:162 | ||||
| chr2:43463265-43463320 | Rare:13 | ||||
| chr2:43595793-43596249 | Common:1; Rare:149 | ||||
| chr2:43637086-43637345 | Common:2; Rare:83 | ||||
| chr2:43676417-43676517 | Rare:32 | ||||
| chr2:43774003-43774445 | Common:4; Rare:145; Clinvar (pathogenic):1 | ||||
| chr2:43995921-43996543 | Common:5; Rare:262; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 |