| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66371568-66371974 | Common:2; Rare:125 | ||||
| chr11:66372163-66372179 | Common:1; Rare:2 | ||||
| chr11:66438596-66438861 | Common:3; Rare:85 | ||||
| chr11:66438992-66439173 | Common:1; Rare:41 | ||||
| chr11:66466671-66467026 | Rare:108 | ||||
| chr11:66467211-66467395 | Common:1; Rare:37 | ||||
| chr11:66479597-66479759 | Common:1; Rare:25 | ||||
| chr11:66479922-66480090 | Common:1; Rare:31 | ||||
| chr11:66480129-66480475 | Common:3; Rare:93 | ||||
| chr11:66480642-66480778 | Common:1; Rare:37 | ||||
| chr11:66510531-66510855 | Common:3; Rare:122; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):4 | ||||
| chr11:66545723-66545818 | Common:1; Rare:25 | ||||
| chr11:66545961-66546273 | Common:5; Rare:82 | ||||
| chr11:66568516-66568768 | Common:5; Rare:80 | ||||
| chr11:66593013-66593275 | Common:1; Rare:92 |