| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:20363650-20363778 | Common:3; Rare:26 | ||||
| chr11:22625801-22626002 | Common:2; Rare:70; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:27363194-27363316 | Rare:45 | ||||
| chr11:27506738-27506879 | Common:1; Rare:59 | ||||
| chr11:28108123-28108414 | Common:1; Rare:87 | ||||
| chr11:30322983-30323186 | Common:2; Rare:59 | ||||
| chr11:31369737-31369888 | Rare:47 | ||||
| chr11:31509575-31509784 | Common:1; Rare:65 | ||||
| chr11:32583663-32583929 | Rare:95 | ||||
| chr11:33039631-33039792 | Rare:39 | ||||
| chr11:33161449-33161678 | Common:6; Rare:63 | ||||
| chr11:33257180-33257413 | Common:2; Rare:78 | ||||
| chr11:33736390-33736553 | Common:2; Rare:54 | ||||
| chr11:34105441-34105717 | Common:4; Rare:91 | ||||
| chr11:34438784-34438997 | Common:2; Rare:71; Clinvar (benign):1 |