| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:1572668-1572753 | Rare:19 | ||||
| chr11:1572918-1572970 | Rare:13 | ||||
| chr11:1753435-1753913 | Common:3; Rare:196; Clinvar:12; Clinvar (benign):21; Clinvar (pathogenic):2 | ||||
| chr11:2912590-2912870 | Rare:61 | ||||
| chr11:3148114-3148453 | Common:5; Rare:68 | ||||
| chr11:3477030-3477097 | Common:1; Rare:20 | ||||
| chr11:3511524-3511697 | Common:3; Rare:38 | ||||
| chr11:6491629-6491668 | Rare:7 | ||||
| chr11:9758130-9758356 | Rare:62 | ||||
| chr11:9759512-9759831 | Common:1; Rare:53 | ||||
| chr11:9775514-9775728 | Common:3; Rare:36 | ||||
| chr11:10303350-10303447 | Rare:13 | ||||
| chr11:10508231-10508245 | Rare:3 | ||||
| chr11:10581949-10582228 | Common:5; Rare:63 | ||||
| chr11:12086690-12086871 | Common:2; Rare:31 |