| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:39437065-39437456 | Common:4; Rare:141 | ||||
| chr2:40511895-40512016 | Rare:22 | ||||
| chr2:40512368-40512829 | Common:3; Rare:91 | ||||
| chr2:42792538-42792800 | Common:3; Rare:72 | ||||
| chr2:43226527-43226865 | Common:3; Rare:146 | ||||
| chr2:43595918-43596205 | Common:1; Rare:101 | ||||
| chr2:43995950-43996276 | Common:5; Rare:145; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:44361484-44362007 | Common:3; Rare:164 | ||||
| chr2:46297721-46297770 | Rare:15 | ||||
| chr2:46543125-46543430 | Rare:80 | ||||
| chr2:46543733-46543776 | Rare:16 | ||||
| chr2:46617025-46617262 | Common:7; Rare:103 | ||||
| chr2:46915722-46915908 | Common:1; Rare:56; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46916012-46916135 | Common:2; Rare:38 | ||||
| chr2:46941715-46941731 | Rare:7; Clinvar (benign):1 |