| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:34051230-34051297 | Common:1; Rare:14 | ||||
| chr11:34051348-34051797 | Rare:143 | ||||
| chr11:34052022-34052503 | Common:5; Rare:207 | ||||
| chr11:34052698-34052847 | Common:1; Rare:51 | ||||
| chr11:34052872-34052904 | Rare:12 | ||||
| chr11:34052970-34053295 | Common:2; Rare:91 | ||||
| chr11:34053298-34053540 | Common:1; Rare:60 | ||||
| chr11:34053698-34054009 | Common:2; Rare:65 | ||||
| chr11:34055260-34055434 | Common:1; Rare:52 | ||||
| chr11:34105009-34105229 | Rare:44 | ||||
| chr11:34105374-34106122 | Common:7; Rare:211 | ||||
| chr11:34106257-34106684 | Common:4; Rare:82 | ||||
| chr11:34357889-34358359 | Common:3; Rare:138 | ||||
| chr11:34358393-34358559 | Rare:35 | ||||
| chr11:34438706-34439092 | Common:2; Rare:128; Clinvar (benign):1 |