| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18698665-18698772 | Common:2; Rare:31 | ||||
| chr11:18791581-18791861 | Common:1; Rare:92 | ||||
| chr11:20387475-20387747 | Common:5; Rare:91 | ||||
| chr11:20669447-20669682 | Common:3; Rare:95 | ||||
| chr11:22337821-22337901 | Rare:17 | ||||
| chr11:22337909-22337968 | Common:1; Rare:18 | ||||
| chr11:22338199-22338434 | Common:1; Rare:48 | ||||
| chr11:22625499-22625609 | Rare:52; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:22625813-22626002 | Common:2; Rare:64; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:24496914-24497235 | Common:3; Rare:86 | ||||
| chr11:26994063-26994139 | Rare:11 | ||||
| chr11:26994173-26994367 | Rare:55 | ||||
| chr11:27363022-27363304 | Common:1; Rare:126 | ||||
| chr11:27472770-27473051 | Common:7; Rare:63 | ||||
| chr11:27506721-27506863 | Common:1; Rare:65 |