| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:3808445-3808606 | Common:1; Rare:47 | ||||
| chr11:3837842-3838040 | Rare:38 | ||||
| chr11:3840903-3841245 | Common:1; Rare:120 | ||||
| chr11:3854487-3854616 | Rare:23 | ||||
| chr11:3855023-3855214 | Common:2; Rare:50 | ||||
| chr11:3855547-3856066 | Common:4; Rare:101 | ||||
| chr11:3856083-3856353 | Rare:79; Clinvar:1 | ||||
| chr11:4094594-4094877 | Common:2; Rare:78 | ||||
| chr11:4393641-4393820 | Common:1; Rare:44 | ||||
| chr11:4608156-4608416 | Common:1; Rare:75 | ||||
| chr11:5226872-5227248 | Common:2; Rare:132; Clinvar:32; Clinvar (benign):4; Clinvar (pathogenic):40 | ||||
| chr11:5624880-5625049 | Rare:29 | ||||
| chr11:5678337-5678662 | Common:1; Rare:66 | ||||
| chr11:5690293-5690382 | Rare:15 | ||||
| chr11:6320490-6320576 | Common:2; Rare:25 |