| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:200812180-200812840 | Common:14; Rare:321 | ||||
| chr2:200864612-200864818 | Rare:153 | ||||
| chr2:200888974-200889511 | Common:6; Rare:314 | ||||
| chr2:200963205-200963314 | Rare:21 | ||||
| chr2:200963219-200963393 | Rare:47 | ||||
| chr2:200963485-200963924 | Common:2; Rare:212 | ||||
| chr2:201071495-201072070 | Rare:241 | ||||
| chr2:201116147-201116443 | Rare:95 | ||||
| chr2:201116615-201117280 | Rare:164 | ||||
| chr2:201118340-201118820 | Rare:108 | ||||
| chr2:201182906-201183187 | Common:3; Rare:71; Clinvar (benign):5 | ||||
| chr2:201233321-201233568 | Common:2; Rare:80 | ||||
| chr2:201257680-201258118 | Common:2; Rare:101 | ||||
| chr2:201260260-201260750 | Common:3; Rare:156 | ||||
| chr2:201451392-201451811 | Common:3; Rare:207 |