| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:3095352-3095419 | Common:1; Rare:15 | ||||
| chr11:3797426-3797939 | Rare:195 | ||||
| chr11:3808494-3808631 | Common:1; Rare:44 | ||||
| chr11:3840899-3841191 | Common:1; Rare:110 | ||||
| chr11:3855555-3855702 | Common:2; Rare:31 | ||||
| chr11:4094614-4095001 | Common:1; Rare:105 | ||||
| chr11:4393666-4393785 | Rare:27 | ||||
| chr11:4608128-4608443 | Common:1; Rare:100 | ||||
| chr11:5596023-5596119 | Rare:28 | ||||
| chr11:5596709-5596806 | Common:1; Rare:33 | ||||
| chr11:5624883-5625029 | Rare:24 | ||||
| chr11:5690285-5690482 | Rare:31 | ||||
| chr11:6319726-6320191 | Common:4; Rare:146 | ||||
| chr11:6320463-6320907 | Common:3; Rare:114 | ||||
| chr11:6390330-6390627 | Common:2; Rare:93; Clinvar:2; Clinvar (benign):1 |