| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:73983210-73983498 | Common:2; Rare:73 | ||||
| chr11:74170845-74171400 | Common:3; Rare:175 | ||||
| chr11:74493224-74493375 | Rare:62; Clinvar (pathogenic):1 | ||||
| chr11:74592492-74592764 | Common:1; Rare:80 | ||||
| chr11:74748635-74748871 | Common:3; Rare:53 | ||||
| chr11:74851571-74851733 | Rare:32 | ||||
| chr11:74949017-74949328 | Common:7; Rare:97 | ||||
| chr11:74988333-74989025 | Common:1; Rare:134 | ||||
| chr11:75240587-75240815 | Common:1; Rare:56 | ||||
| chr11:75351603-75351868 | Common:3; Rare:78 | ||||
| chr11:75399461-75399595 | Common:4; Rare:73 | ||||
| chr11:75562724-75562883 | Common:1; Rare:31 | ||||
| chr11:75668070-75668212 | Common:1; Rare:41 | ||||
| chr11:75668915-75668947 | Rare:9 | ||||
| chr11:75768647-75768746 | Common:1; Rare:26 |