| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:2902059-2902387 | Common:1; Rare:74 | ||||
| chr11:2992247-2992516 | Common:2; Rare:104 | ||||
| chr11:3057354-3057553 | Rare:71 | ||||
| chr11:3165263-3165487 | Common:2; Rare:79 | ||||
| chr11:3379082-3379302 | Common:3; Rare:57 | ||||
| chr11:3797455-3797691 | Rare:95 | ||||
| chr11:3808477-3808601 | Common:1; Rare:37 | ||||
| chr11:3840910-3841076 | Rare:73 | ||||
| chr11:3855535-3855711 | Common:2; Rare:36 | ||||
| chr11:4094718-4094897 | Common:1; Rare:52 | ||||
| chr11:4608103-4608405 | Common:1; Rare:99 | ||||
| chr11:5505633-5505782 | Common:1; Rare:46 | ||||
| chr11:5624876-5625052 | Rare:33 | ||||
| chr11:6234620-6234968 | Common:2; Rare:91 | ||||
| chr11:6390237-6390603 | Common:3; Rare:113; Clinvar:1; Clinvar (benign):1 |