| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:71448321-71448715 | Common:4; Rare:104; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:71452987-71453284 | Common:3; Rare:83 | ||||
| chr11:71787303-71787548 | Common:15; Rare:93 | ||||
| chr11:71928268-71928464 | Rare:48 | ||||
| chr11:71928568-71928703 | Rare:32 | ||||
| chr11:71928887-71929076 | Common:1; Rare:63 | ||||
| chr11:72041006-72041299 | Common:1; Rare:57 | ||||
| chr11:72041512-72041614 | Rare:13 | ||||
| chr11:72041846-72041929 | Common:2; Rare:19 | ||||
| chr11:72041936-72042071 | Rare:30 | ||||
| chr11:72080319-72080341 | Rare:2 | ||||
| chr11:72080436-72080861 | Common:2; Rare:99; Clinvar:8 | ||||
| chr11:72098817-72098891 | Rare:23 | ||||
| chr11:72103204-72103513 | Rare:87 | ||||
| chr11:72112182-72112520 | Rare:88 |