| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:60870421-60870512 | Rare:22 | ||||
| chr11:60906394-60906696 | Common:1; Rare:83 | ||||
| chr11:60914037-60914210 | Common:1; Rare:46 | ||||
| chr11:60914343-60914499 | Rare:42 | ||||
| chr11:61161176-61161755 | Common:1; Rare:156 | ||||
| chr11:61302252-61302623 | Rare:104 | ||||
| chr11:61332910-61333372 | Common:1; Rare:151 | ||||
| chr11:61356839-61356980 | Common:1; Rare:32 | ||||
| chr11:61361810-61362055 | Common:2; Rare:57; Clinvar:2 | ||||
| chr11:61362212-61362433 | Common:2; Rare:62; Clinvar:8; Clinvar (benign):1 | ||||
| chr11:61392517-61392649 | Common:2; Rare:44; Clinvar:3; Clinvar (benign):2 | ||||
| chr11:61429185-61429490 | Common:3; Rare:97 | ||||
| chr11:61429863-61430187 | Common:1; Rare:137; Clinvar:3; Clinvar (benign):7 | ||||
| chr11:61481052-61481208 | Rare:28 | ||||
| chr11:61680202-61680453 | Common:1; Rare:76 |