| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:20387475-20387771 | Common:5; Rare:96 | ||||
| chr11:22625808-22625955 | Common:2; Rare:54; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:27363119-27363393 | Rare:117 | ||||
| chr11:27506738-27506864 | Common:1; Rare:53 | ||||
| chr11:28108110-28108402 | Common:1; Rare:87 | ||||
| chr11:30322974-30323164 | Common:1; Rare:55 | ||||
| chr11:31509567-31509784 | Common:1; Rare:67 | ||||
| chr11:33161435-33161678 | Common:6; Rare:68 | ||||
| chr11:33257210-33257427 | Common:3; Rare:73 | ||||
| chr11:33722663-33722844 | Common:2; Rare:34 | ||||
| chr11:33736390-33736605 | Common:2; Rare:66 | ||||
| chr11:34052159-34052451 | Common:4; Rare:140 | ||||
| chr11:34105462-34105682 | Common:3; Rare:74 | ||||
| chr11:34438706-34439007 | Common:2; Rare:101; Clinvar (benign):1 | ||||
| chr11:34916311-34916650 | Common:9; Rare:139; Clinvar:4; Clinvar (benign):10; Clinvar (pathogenic):1 |