| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18394397-18394726 | Common:1; Rare:121; Clinvar (benign):1 | ||||
| chr11:18526803-18527063 | Common:3; Rare:119 | ||||
| chr11:18588656-18588905 | Common:2; Rare:90 | ||||
| chr11:18634283-18634566 | Common:3; Rare:98 | ||||
| chr11:18634753-18634838 | Rare:27 | ||||
| chr11:18698515-18698764 | Common:4; Rare:63 | ||||
| chr11:19713863-19714195 | Rare:95 | ||||
| chr11:20363656-20363753 | Common:1; Rare:22 | ||||
| chr11:20387399-20387794 | Common:8; Rare:129 | ||||
| chr11:22625508-22625615 | Rare:54; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:22625796-22626091 | Common:3; Rare:84; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:22666940-22667052 | Rare:32 | ||||
| chr11:22829321-22829433 | Common:1; Rare:28 | ||||
| chr11:22829744-22830175 | Common:4; Rare:133 | ||||
| chr11:27506716-27506877 | Common:1; Rare:75 |