| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:8719241-8719435 | Common:1; Rare:38 | ||||
| chr11:8871234-8871499 | Rare:54 | ||||
| chr11:8910927-8911274 | Common:7; Rare:95 | ||||
| chr11:8964218-8964523 | Common:4; Rare:119 | ||||
| chr11:8964717-8965038 | Common:3; Rare:76 | ||||
| chr11:9144828-9145077 | Common:1; Rare:62 | ||||
| chr11:9460601-9461059 | Common:4; Rare:115 | ||||
| chr11:9573358-9573636 | Common:2; Rare:81 | ||||
| chr11:9575261-9575796 | Common:2; Rare:110 | ||||
| chr11:9664000-9664228 | Common:4; Rare:83 | ||||
| chr11:10294198-10294464 | Common:2; Rare:73 | ||||
| chr11:10294549-10294773 | Rare:52 | ||||
| chr11:10304801-10305138 | Common:1; Rare:78 | ||||
| chr11:10455134-10455432 | Common:5; Rare:55; Clinvar:2; Clinvar (benign):6 | ||||
| chr11:10455886-10456067 | Rare:29 |