| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:34916292-34916658 | Common:10; Rare:148; Clinvar:5; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:35138954-35139310 | Common:1; Rare:94 | ||||
| chr11:35662667-35662950 | Common:3; Rare:88 | ||||
| chr11:36289372-36289531 | Common:2; Rare:61 | ||||
| chr11:36300808-36300890 | Common:1; Rare:10 | ||||
| chr11:36376260-36376749 | Common:5; Rare:100 | ||||
| chr11:36377387-36377790 | Common:3; Rare:93 | ||||
| chr11:36377991-36378316 | Rare:70 | ||||
| chr11:36510236-36510372 | Rare:38 | ||||
| chr11:43358802-43359106 | Rare:123 | ||||
| chr11:43880735-43881120 | Common:5; Rare:86 | ||||
| chr11:44066195-44066548 | Common:3; Rare:85 | ||||
| chr11:45804974-45805211 | Common:3; Rare:65; Clinvar:4; Clinvar (benign):1 | ||||
| chr11:45847215-45847493 | Common:2; Rare:112 | ||||
| chr11:45917815-45918172 | Common:1; Rare:91; Clinvar:2; Clinvar (benign):1 |