| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:61177257-61177590 | Common:6; Rare:138 | ||||
| chr2:61177972-61178217 | Common:1; Rare:80 | ||||
| chr2:61178967-61179109 | Common:2; Rare:43 | ||||
| chr2:61184505-61184791 | Common:1; Rare:73 | ||||
| chr2:61185502-61185887 | Common:1; Rare:142 | ||||
| chr2:61185944-61186188 | Common:2; Rare:65 | ||||
| chr2:61203941-61204041 | Rare:18 | ||||
| chr2:61470661-61471033 | Common:1; Rare:122 | ||||
| chr2:61471074-61471370 | Common:2; Rare:110 | ||||
| chr2:61536624-61536762 | Rare:42 | ||||
| chr2:61537740-61537778 | Rare:3 | ||||
| chr2:61537811-61538126 | Common:3; Rare:76 | ||||
| chr2:61538207-61538427 | Common:1; Rare:51 | ||||
| chr2:61854004-61854186 | Common:2; Rare:79; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:61888370-61888744 | Common:1; Rare:167 |