| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:34621845-34622245 | Common:5; Rare:89 | ||||
| chr11:34915171-34916280 | Common:22; Rare:468; Clinvar (benign):3 | ||||
| chr11:34916254-34916745 | Common:82; Rare:1201; Clinvar:43; Clinvar (benign):89; Clinvar (pathogenic):7 | ||||
| chr11:34916860-34917260 | Common:4; Rare:102 | ||||
| chr11:35138843-35139243 | Common:3; Rare:143 | ||||
| chr11:35618010-35618420 | Common:5; Rare:104 | ||||
| chr11:35618710-35618950 | Common:1; Rare:80 | ||||
| chr11:35662480-35663670 | Common:12; Rare:1229; Clinvar (pathogenic):1 | ||||
| chr11:35943809-35944570 | Common:10; Rare:381 | ||||
| chr11:36289269-36289669 | Common:9; Rare:306 | ||||
| chr11:36398387-36398806 | Common:12; Rare:119 | ||||
| chr11:36509700-36510100 | Common:1; Rare:180 | ||||
| chr11:36510169-36510440 | Common:3; Rare:384 | ||||
| chr11:36594218-36594618 | Common:5; Rare:151 | ||||
| chr11:43311712-43312112 | Common:6; Rare:319 |