| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:144519348-144519433 | Rare:9 | ||||
| chr2:147922875-147923002 | Common:1; Rare:24 | ||||
| chr2:149161344-149161535 | Common:2; Rare:20 | ||||
| chr2:149575709-149575942 | Common:1; Rare:69; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:152390065-152390335 | Rare:53 | ||||
| chr2:156254893-156255291 | Common:4; Rare:101 | ||||
| chr2:156326801-156327062 | Rare:64 | ||||
| chr2:156334435-156334790 | Common:1; Rare:81 | ||||
| chr2:158497226-158497481 | Common:3; Rare:46 | ||||
| chr2:159614141-159614214 | Rare:8 | ||||
| chr2:159764935-159765258 | Common:3; Rare:53 | ||||
| chr2:159766192-159766330 | Rare:23 | ||||
| chr2:159766940-159767401 | Common:3; Rare:102 | ||||
| chr2:159780016-159780460 | Common:2; Rare:122 | ||||
| chr2:159780950-159781098 | Common:1; Rare:47 |