| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66268337-66268710 | Common:3; Rare:106 | ||||
| chr11:66268744-66268929 | Common:2; Rare:55 | ||||
| chr11:66288973-66289474 | Common:2; Rare:129 | ||||
| chr11:66289593-66289653 | Rare:12 | ||||
| chr11:66317451-66317594 | Rare:44 | ||||
| chr11:66344984-66345283 | Common:1; Rare:81 | ||||
| chr11:66347550-66347923 | Common:6; Rare:89; Clinvar (benign):2 | ||||
| chr11:66348023-66348227 | Common:1; Rare:100 | ||||
| chr11:66371686-66372069 | Common:2; Rare:95 | ||||
| chr11:66372100-66372221 | Common:2; Rare:26 | ||||
| chr11:66372453-66372566 | Rare:19 | ||||
| chr11:66438747-66439122 | Common:2; Rare:97 | ||||
| chr11:66466637-66466932 | Rare:87 | ||||
| chr11:66479926-66480016 | Rare:17 | ||||
| chr11:66480134-66480560 | Common:4; Rare:106 |