| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:68038915-68039078 | Rare:50; Clinvar:1 | ||||
| chr11:68271871-68272146 | Common:2; Rare:115 | ||||
| chr11:68460556-68460793 | Common:3; Rare:86 | ||||
| chr11:68903759-68903955 | Common:5; Rare:90; Clinvar:1; Clinvar (benign):7 | ||||
| chr11:69048701-69048995 | Common:6; Rare:107 | ||||
| chr11:69293995-69294184 | Common:2; Rare:23 | ||||
| chr11:69640972-69641418 | Common:1; Rare:110 | ||||
| chr11:69641434-69641511 | Rare:15 | ||||
| chr11:69675300-69675519 | Rare:60 | ||||
| chr11:70078395-70078604 | Rare:54 | ||||
| chr11:70203133-70203355 | Common:3; Rare:85 | ||||
| chr11:70398421-70398614 | Common:2; Rare:73 | ||||
| chr11:70414317-70414652 | Common:4; Rare:87 | ||||
| chr11:71448352-71448673 | Common:3; Rare:83; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:71787355-71787557 | Common:13; Rare:89 |