| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:1231706-1232028 | Common:1; Rare:67 | ||||
| chr11:1236229-1236562 | Common:1; Rare:118; Clinvar (benign):1 | ||||
| chr11:1255190-1255444 | Common:6; Rare:89; Clinvar (benign):2 | ||||
| chr11:2595518-2595847 | Common:5; Rare:63 | ||||
| chr11:2631264-2631428 | Common:1; Rare:33 | ||||
| chr11:2639086-2639128 | Rare:8 | ||||
| chr11:2642918-2642989 | Rare:7 | ||||
| chr11:2643651-2643943 | Rare:56 | ||||
| chr11:2644498-2644526 | Rare:9 | ||||
| chr11:2644790-2644960 | Rare:31 | ||||
| chr11:2646004-2646255 | Common:2; Rare:39 | ||||
| chr11:2647717-2647970 | Common:1; Rare:36 | ||||
| chr11:2649940-2649976 | Rare:10 | ||||
| chr11:2650496-2650769 | Rare:47 | ||||
| chr11:2652795-2653010 | Rare:35 |