| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:47449086-47449247 | Rare:37; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47565460-47565616 | Common:2; Rare:31 | ||||
| chr11:47578968-47579085 | Rare:60; Clinvar:2 | ||||
| chr11:59142721-59142859 | Rare:20 | ||||
| chr11:61333065-61333259 | Rare:62 | ||||
| chr11:61361875-61361964 | Common:1; Rare:19 | ||||
| chr11:61362263-61362410 | Common:1; Rare:43; Clinvar:7 | ||||
| chr11:61429935-61430140 | Common:1; Rare:93; Clinvar (benign):2 | ||||
| chr11:61792581-61792944 | Common:5; Rare:91 | ||||
| chr11:62665156-62665317 | Common:4; Rare:69 | ||||
| chr11:62679030-62679174 | Rare:45 | ||||
| chr11:62855882-62856079 | Rare:80 | ||||
| chr11:64226152-64226297 | Common:2; Rare:41 | ||||
| chr11:64318004-64318282 | Rare:117 | ||||
| chr11:65014063-65014201 | Rare:28 |