| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:834811-835368 | Common:11; Rare:314 | ||||
| chr11:842478-842873 | Common:7; Rare:169 | ||||
| chr11:843853-844159 | Common:2; Rare:82 | ||||
| chr11:910794-911315 | Common:6; Rare:187 | ||||
| chr11:925693-925896 | Common:2; Rare:85 | ||||
| chr11:1309393-1309953 | Common:4; Rare:193 | ||||
| chr11:1389501-1389942 | Common:2; Rare:113 | ||||
| chr11:1571970-1572131 | Rare:53 | ||||
| chr11:1572262-1572397 | Rare:36 | ||||
| chr11:1763860-1764150 | Common:3; Rare:127; Clinvar:4; Clinvar (benign):6 | ||||
| chr11:1830684-1831084 | Common:2; Rare:159 | ||||
| chr11:1834216-1834359 | Rare:30 | ||||
| chr11:1863000-1863480 | Common:3; Rare:108 | ||||
| chr11:1863578-1863723 | Rare:40 | ||||
| chr11:2137279-2137456 | Rare:45 |