| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:39120320-39120570 | Common:1; Rare:165; Clinvar:4; Clinvar (benign):16 | ||||
| chr2:39120618-39121204 | Common:4; Rare:340 | ||||
| chr2:39121308-39121615 | Common:1; Rare:110 | ||||
| chr2:39124159-39124604 | Common:3; Rare:394 | ||||
| chr2:39436031-39436905 | Common:16; Rare:580 | ||||
| chr2:39436887-39437505 | Common:12; Rare:481 | ||||
| chr2:39778700-39778979 | Common:2; Rare:92 | ||||
| chr2:39779101-39779409 | Common:11; Rare:225 | ||||
| chr2:40452020-40452330 | Common:14; Rare:204 | ||||
| chr2:42169109-42169526 | Common:3; Rare:460 | ||||
| chr2:42169490-42169980 | Common:4; Rare:212 | ||||
| chr2:42359847-42360479 | Rare:258 | ||||
| chr2:42360478-42360978 | Common:3; Rare:153 | ||||
| chr2:42361454-42361838 | Common:5; Rare:112 | ||||
| chr2:42493810-42494177 | Common:2; Rare:317 |