| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:43680404-43680822 | Common:3; Rare:113 | ||||
| chr11:43833703-43834040 | Common:2; Rare:59 | ||||
| chr11:43880690-43880884 | Common:2; Rare:45 | ||||
| chr11:44950151-44950231 | Common:1; Rare:23 | ||||
| chr11:44950881-44951133 | Rare:61 | ||||
| chr11:45147182-45147373 | Common:1; Rare:76 | ||||
| chr11:45286181-45286437 | Rare:78 | ||||
| chr11:45804965-45805170 | Common:2; Rare:48; Clinvar:4 | ||||
| chr11:45847190-45847491 | Common:2; Rare:123 | ||||
| chr11:45885460-45885839 | Common:3; Rare:105 | ||||
| chr11:45917818-45918190 | Common:1; Rare:97; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:46120934-46121253 | Common:2; Rare:45 | ||||
| chr11:46381975-46382117 | Common:1; Rare:57 | ||||
| chr11:46382133-46382342 | Rare:72 | ||||
| chr11:46593985-46594133 | Common:2; Rare:36 |