| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74472422-74472908 | Common:5; Rare:215 | ||||
| chr2:74482599-74482650 | Rare:17 | ||||
| chr2:74482668-74482708 | Rare:20 | ||||
| chr2:74482887-74483125 | Common:1; Rare:88 | ||||
| chr2:74483291-74483426 | Common:2; Rare:52 | ||||
| chr2:74507252-74507477 | Rare:60 | ||||
| chr2:74507614-74508120 | Common:2; Rare:135 | ||||
| chr2:74529392-74529508 | Common:1; Rare:43; Clinvar (benign):2 | ||||
| chr2:74529608-74529770 | Rare:76; Clinvar:2 | ||||
| chr2:74529806-74530043 | Rare:58; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:74530498-74530622 | Common:1; Rare:43; Clinvar:2 | ||||
| chr2:74548985-74549066 | Rare:22 | ||||
| chr2:74554073-74554193 | Rare:31 | ||||
| chr2:74554406-74554831 | Common:3; Rare:136 | ||||
| chr2:74654089-74654301 | Common:1; Rare:55 |