| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65478857-65479078 | Rare:92 | ||||
| chr11:65487590-65487990 | Common:1; Rare:71 | ||||
| chr11:65489011-65490032 | Common:17; Rare:283 | ||||
| chr11:65493821-65494221 | Common:3; Rare:77 | ||||
| chr11:65497348-65497843 | Common:2; Rare:410 | ||||
| chr11:65498555-65498708 | Common:1; Rare:96 | ||||
| chr11:65498905-65499143 | Common:1; Rare:177 | ||||
| chr11:65499440-65499970 | Common:3; Rare:275 | ||||
| chr11:65500569-65501010 | Common:2; Rare:217 | ||||
| chr11:65616535-65616822 | Common:2; Rare:190 | ||||
| chr11:65652961-65653094 | Common:1; Rare:48 | ||||
| chr11:66269210-66269690 | Rare:184 | ||||
| chr11:66313570-66313820 | Common:4; Rare:60 | ||||
| chr11:66351318-66351540 | Rare:65 | ||||
| chr11:66868598-66869230 | Common:2; Rare:192; Clinvar:2; Clinvar (benign):6 |