| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:46120941-46121037 | Rare:9 | ||||
| chr11:46121069-46121303 | Common:2; Rare:40 | ||||
| chr11:46277903-46278114 | Rare:57 | ||||
| chr11:46380706-46380996 | Common:1; Rare:82 | ||||
| chr11:46617148-46617607 | Common:5; Rare:134 | ||||
| chr11:46700549-46700818 | Common:1; Rare:70 | ||||
| chr11:46700904-46701068 | Common:3; Rare:42 | ||||
| chr11:46846218-46846414 | Common:1; Rare:54 | ||||
| chr11:46936682-46936826 | Common:2; Rare:50 | ||||
| chr11:47172375-47172414 | Rare:8 | ||||
| chr11:47186382-47186544 | Rare:47 | ||||
| chr11:47214350-47214496 | Common:1; Rare:13 | ||||
| chr11:47214832-47215123 | Common:2; Rare:75; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:47248765-47248938 | Rare:69 | ||||
| chr11:47269560-47269714 | Common:1; Rare:51 |