| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:62545640-62546160 | Common:1; Rare:114 | ||||
| chr11:62546799-62547067 | Common:1; Rare:82 | ||||
| chr11:62573175-62573638 | Common:2; Rare:198 | ||||
| chr11:62573825-62574237 | Rare:137 | ||||
| chr11:62591483-62591916 | Rare:145 | ||||
| chr11:62600497-62600897 | Common:1; Rare:136 | ||||
| chr11:62601087-62601617 | Common:4; Rare:258 | ||||
| chr11:62601736-62602011 | Common:1; Rare:92 | ||||
| chr11:62612406-62613193 | Common:8; Rare:410; Clinvar:9; Clinvar (benign):8 | ||||
| chr11:62621940-62622263 | Common:2; Rare:99 | ||||
| chr11:62646567-62646814 | Common:1; Rare:100; Clinvar (pathogenic):1 | ||||
| chr11:62653259-62653447 | Common:1; Rare:64 | ||||
| chr11:62665122-62665507 | Common:6; Rare:181 | ||||
| chr11:62671525-62671888 | Rare:132; Clinvar (benign):1 | ||||
| chr11:62678225-62678625 | Rare:199 |