| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:34438784-34439076 | Common:2; Rare:98; Clinvar (benign):1 | ||||
| chr11:34620867-34621155 | Common:2; Rare:59 | ||||
| chr11:34632506-34632598 | Rare:13 | ||||
| chr11:34916287-34916719 | Common:11; Rare:176; Clinvar:7; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chr11:35138949-35139369 | Common:1; Rare:116 | ||||
| chr11:35662636-35662968 | Common:3; Rare:105 | ||||
| chr11:35943949-35944128 | Common:2; Rare:65 | ||||
| chr11:36289372-36289539 | Common:2; Rare:62 | ||||
| chr11:36510229-36510377 | Rare:45 | ||||
| chr11:36598207-36598547 | Common:3; Rare:67; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:43358795-43358983 | Rare:92 | ||||
| chr11:43680500-43680893 | Common:1; Rare:125 | ||||
| chr11:43880755-43881109 | Common:5; Rare:80 | ||||
| chr11:44066189-44066530 | Common:3; Rare:87 | ||||
| chr11:44565261-44565687 | Common:3; Rare:104 |