| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:34051601-34051741 | Rare:59 | ||||
| chr11:34052038-34052630 | Common:5; Rare:250 | ||||
| chr11:34053057-34053088 | Rare:7 | ||||
| chr11:34053239-34053560 | Common:2; Rare:89 | ||||
| chr11:34055584-34055756 | Common:1; Rare:32 | ||||
| chr11:34105493-34105724 | Common:2; Rare:76 | ||||
| chr11:34105970-34106033 | Rare:13 | ||||
| chr11:34438784-34439015 | Common:2; Rare:80; Clinvar (benign):1 | ||||
| chr11:34916024-34916089 | Common:1; Rare:23 | ||||
| chr11:34916251-34916723 | Common:13; Rare:190; Clinvar:8; Clinvar (benign):14; Clinvar (pathogenic):1 | ||||
| chr11:35662639-35662950 | Common:3; Rare:96 | ||||
| chr11:35943969-35944110 | Common:2; Rare:46 | ||||
| chr11:36289362-36289505 | Common:1; Rare:56 | ||||
| chr11:36510214-36510382 | Rare:57 | ||||
| chr11:36594338-36594835 | Common:2; Rare:87 |