| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65911710-65912110 | Common:3; Rare:132 | ||||
| chr11:65915551-65915943 | Common:3; Rare:148 | ||||
| chr11:66015400-66015840 | Common:4; Rare:142 | ||||
| chr11:66269220-66269760 | Rare:113 | ||||
| chr11:66312130-66312670 | Common:8; Rare:159 | ||||
| chr11:66312682-66313082 | Common:6; Rare:156 | ||||
| chr11:66328310-66328736 | Common:3; Rare:138 | ||||
| chr11:66621972-66622220 | Common:1; Rare:45 | ||||
| chr11:66708160-66708610 | Common:3; Rare:114; Clinvar:3; Clinvar (benign):2 | ||||
| chr11:66727260-66728134 | Common:3; Rare:258 | ||||
| chr11:66728046-66728246 | Rare:50 | ||||
| chr11:66858785-66859739 | Common:2; Rare:534 | ||||
| chr11:66870416-66870873 | Common:2; Rare:178; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:66905990-66906300 | Common:5; Rare:89 | ||||
| chr11:66933510-66933923 | Common:3; Rare:128 |