| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:6614876-6615332 | Common:2; Rare:128; Clinvar:17; Clinvar (benign):8; Clinvar (pathogenic):5 | ||||
| chr11:7513630-7513791 | Common:2; Rare:50 | ||||
| chr11:8682626-8682798 | Common:2; Rare:74 | ||||
| chr11:8964384-8964535 | Common:3; Rare:46 | ||||
| chr11:8964920-8965018 | Common:1; Rare:26 | ||||
| chr11:9460624-9461035 | Common:4; Rare:106 | ||||
| chr11:9664000-9664119 | Common:3; Rare:40 | ||||
| chr11:10455921-10456080 | Rare:21 | ||||
| chr11:10541133-10541345 | Rare:79 | ||||
| chr11:10800202-10800834 | Common:2; Rare:177 | ||||
| chr11:10802049-10802408 | Common:1; Rare:102 | ||||
| chr11:10808810-10809130 | Common:1; Rare:126 | ||||
| chr11:10858023-10858309 | Common:2; Rare:90 | ||||
| chr11:14643627-14643761 | Common:1; Rare:61 | ||||
| chr11:16738447-16738751 | Common:3; Rare:70 |