| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:74948973-74949358 | Common:14; Rare:211 | ||||
| chr11:74988720-74989011 | Rare:118 | ||||
| chr11:75351585-75351868 | Common:5; Rare:126 | ||||
| chr11:75399395-75399649 | Common:9; Rare:189 | ||||
| chr11:75430050-75430349 | Common:2; Rare:193 | ||||
| chr11:75430420-75431000 | Common:6; Rare:247 | ||||
| chr11:75525828-75526171 | Common:4; Rare:188 | ||||
| chr11:75562051-75562480 | Common:2; Rare:148; Clinvar:8; Clinvar (benign):4 | ||||
| chr11:75562680-75562865 | Common:2; Rare:89 | ||||
| chr11:75768441-75768781 | Common:4; Rare:178 | ||||
| chr11:75814690-75814860 | Rare:58 | ||||
| chr11:75814868-75815438 | Common:5; Rare:271 | ||||
| chr11:76206240-76206760 | Common:11; Rare:259 | ||||
| chr11:76381029-76381423 | Common:8; Rare:219 | ||||
| chr11:76444240-76444500 | Common:2; Rare:108 |