| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:68460223-68460402 | Common:3; Rare:64 | ||||
| chr11:68460538-68460793 | Common:6; Rare:192 | ||||
| chr11:68839208-68839608 | Common:4; Rare:159 | ||||
| chr11:68903753-68903977 | Common:10; Rare:187; Clinvar:6; Clinvar (benign):14 | ||||
| chr11:69048690-69048993 | Common:6; Rare:107 | ||||
| chr11:69640970-69641253 | Common:2; Rare:114 | ||||
| chr11:69668020-69668590 | Common:4; Rare:204 | ||||
| chr11:69675278-69675513 | Rare:125 | ||||
| chr11:70203092-70203377 | Common:8; Rare:206 | ||||
| chr11:70270452-70270786 | Common:4; Rare:260 | ||||
| chr11:70371170-70371720 | Common:16; Rare:95 | ||||
| chr11:70398237-70398630 | Common:7; Rare:249 | ||||
| chr11:71252330-71252758 | Common:4; Rare:146 | ||||
| chr11:71252682-71253018 | Common:5; Rare:122 | ||||
| chr11:71448277-71448717 | Common:8; Rare:232; Clinvar:7; Clinvar (benign):2 |