| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:20387382-20387794 | Common:16; Rare:249 | ||||
| chr11:22625410-22625720 | Common:4; Rare:194; Clinvar:17; Clinvar (benign):7; Clinvar (pathogenic):4 | ||||
| chr11:22625742-22626021 | Common:5; Rare:174; Clinvar:7; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr11:22666475-22666879 | Common:2; Rare:125 | ||||
| chr11:22666828-22667106 | Common:2; Rare:129 | ||||
| chr11:22674567-22674973 | Common:7; Rare:128 | ||||
| chr11:27363036-27363399 | Common:1; Rare:300 | ||||
| chr11:27471950-27472420 | Common:6; Rare:194 | ||||
| chr11:27472652-27473041 | Common:8; Rare:179 | ||||
| chr11:27506748-27506893 | Common:2; Rare:113 | ||||
| chr11:28108085-28108424 | Common:2; Rare:183 | ||||
| chr11:30322937-30323180 | Common:4; Rare:124 | ||||
| chr11:31369737-31369905 | Rare:52 | ||||
| chr11:31509530-31509946 | Common:3; Rare:292 | ||||
| chr11:32090808-32091158 | Common:3; Rare:104 |