| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:2167923-2168176 | Common:1; Rare:80; Clinvar:6; Clinvar (benign):3 | ||||
| chr11:2168967-2169228 | Common:3; Rare:59 | ||||
| chr11:2171696-2171942 | Rare:77; Clinvar:9; Clinvar (pathogenic):3 | ||||
| chr11:2444484-2444708 | Rare:35 | ||||
| chr11:2461286-2461538 | Common:1; Rare:79 | ||||
| chr11:3057365-3057546 | Rare:64 | ||||
| chr11:3379082-3379339 | Common:4; Rare:69 | ||||
| chr11:3641984-3642202 | Common:8; Rare:77 | ||||
| chr11:3797482-3797736 | Rare:101 | ||||
| chr11:3808534-3808595 | Common:1; Rare:22 | ||||
| chr11:3840903-3841040 | Rare:61 | ||||
| chr11:3855547-3855792 | Common:2; Rare:47 | ||||
| chr11:3856226-3856265 | Rare:13 | ||||
| chr11:4094559-4094712 | Common:1; Rare:42 | ||||
| chr11:4094718-4094893 | Common:1; Rare:51 |