| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:43312298-43312698 | Common:5; Rare:122 | ||||
| chr11:43358704-43359392 | Rare:933 | ||||
| chr11:43643639-43644390 | Common:9; Rare:238 | ||||
| chr11:43644322-43644722 | Common:1; Rare:86 | ||||
| chr11:43680370-43680840 | Common:7; Rare:323 | ||||
| chr11:43680975-43681760 | Common:10; Rare:308 | ||||
| chr11:43880610-43880920 | Common:10; Rare:305 | ||||
| chr11:43941821-43942221 | Common:14; Rare:81 | ||||
| chr11:43942340-43942690 | Common:12; Rare:216 | ||||
| chr11:44065920-44067395 | Common:35; Rare:949 | ||||
| chr11:44067402-44067692 | Common:4; Rare:122 | ||||
| chr11:44095406-44095806 | Common:5; Rare:185; Clinvar (benign):9 | ||||
| chr11:44096032-44096432 | Common:2; Rare:170 | ||||
| chr11:44309280-44309680 | Rare:93 | ||||
| chr11:44309768-44310440 | Common:14; Rare:439; Clinvar:7; Clinvar (benign):18; Clinvar (pathogenic):2 |