| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:130069593-130069998 | Common:2; Rare:152 | ||||
| chr11:130314271-130314520 | Common:1; Rare:82 | ||||
| chr11:130314784-130315085 | Common:4; Rare:108 | ||||
| chr11:130893025-130893170 | Common:2; Rare:26 | ||||
| chr11:130910016-130910299 | Common:1; Rare:81 | ||||
| chr11:130916403-130916558 | Common:4; Rare:58 | ||||
| chr11:133845396-133845640 | Common:1; Rare:66 | ||||
| chr11:133952014-133952267 | Common:1; Rare:77 | ||||
| chr11:133956989-133957105 | Common:1; Rare:41 | ||||
| chr11:134068746-134069111 | Common:2; Rare:135; Clinvar (pathogenic):1 | ||||
| chr11:134223867-134224111 | Common:2; Rare:86 | ||||
| chr11:134224533-134224690 | Rare:58 | ||||
| chr11:134225448-134225475 | Rare:8 | ||||
| chr11:134253290-134253617 | Common:2; Rare:123; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:134276195-134276266 | Common:1; Rare:10 |