| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:62771213-62771399 | Rare:46 | ||||
| chr11:62832038-62832214 | Rare:63 | ||||
| chr11:62841800-62842097 | Common:6; Rare:122 | ||||
| chr11:62855881-62856116 | Rare:91 | ||||
| chr11:62921322-62921429 | Rare:24 | ||||
| chr11:63681251-63681691 | Common:2; Rare:173 | ||||
| chr11:64226141-64226314 | Common:2; Rare:46 | ||||
| chr11:64240891-64241169 | Rare:78 | ||||
| chr11:64284560-64284817 | Rare:108 | ||||
| chr11:64285704-64285871 | Rare:56 | ||||
| chr11:64317456-64317660 | Common:3; Rare:75 | ||||
| chr11:64318067-64318300 | Rare:103 | ||||
| chr11:64643333-64643405 | Common:1; Rare:10 | ||||
| chr11:64778419-64778728 | Common:2; Rare:138 | ||||
| chr11:64810495-64810806 | Common:2; Rare:73; Clinvar:1; Clinvar (benign):2 |