| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74199084-74199345 | Rare:54 | ||||
| chr2:74290040-74290350 | Common:1; Rare:50 | ||||
| chr2:74391651-74392351 | Common:10; Rare:608 | ||||
| chr2:74421487-74421813 | Rare:255 | ||||
| chr2:74440440-74440880 | Rare:153 | ||||
| chr2:74441807-74442120 | Common:6; Rare:148 | ||||
| chr2:74454816-74455164 | Rare:183 | ||||
| chr2:74455108-74456268 | Common:3; Rare:837 | ||||
| chr2:74457917-74458525 | Common:3; Rare:494 | ||||
| chr2:74458940-74459536 | Common:4; Rare:312 | ||||
| chr2:74465207-74465583 | Common:5; Rare:222; Clinvar:3; Clinvar (benign):6 | ||||
| chr2:74472112-74472262 | Rare:57 | ||||
| chr2:74472282-74472920 | Common:13; Rare:638 | ||||
| chr2:74482122-74482272 | Rare:100 | ||||
| chr2:74482851-74483132 | Common:3; Rare:264 |