| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:71448342-71448606 | Common:3; Rare:71; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:71452991-71453261 | Common:3; Rare:77 | ||||
| chr11:71479950-71480156 | Rare:47 | ||||
| chr11:72112232-72112494 | Rare:66 | ||||
| chr11:72752382-72752532 | Common:3; Rare:47 | ||||
| chr11:72793583-72793813 | Common:1; Rare:55 | ||||
| chr11:72814039-72814452 | Common:4; Rare:123 | ||||
| chr11:73308111-73308284 | Common:1; Rare:63 | ||||
| chr11:73787862-73787934 | Common:1; Rare:18 | ||||
| chr11:73876792-73877037 | Common:4; Rare:70 | ||||
| chr11:73983200-73983520 | Common:4; Rare:79 | ||||
| chr11:74170987-74171341 | Common:2; Rare:116 | ||||
| chr11:74398385-74398558 | Common:3; Rare:38 | ||||
| chr11:74748656-74748886 | Common:3; Rare:55 | ||||
| chr11:74949054-74949310 | Common:6; Rare:75 |