| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:62591440-62591957 | Rare:445 | ||||
| chr11:62600129-62601119 | Common:5; Rare:498 | ||||
| chr11:62601199-62601431 | Common:1; Rare:128 | ||||
| chr11:62601541-62602038 | Common:6; Rare:424 | ||||
| chr11:62611440-62611900 | Rare:201 | ||||
| chr11:62611992-62612670 | Common:7; Rare:255 | ||||
| chr11:62612685-62612892 | Common:1; Rare:148; Clinvar:6; Clinvar (benign):4 | ||||
| chr11:62612960-62613230 | Rare:63; Clinvar:1 | ||||
| chr11:62621664-62622388 | Common:9; Rare:457 | ||||
| chr11:62639667-62639842 | Common:2; Rare:56 | ||||
| chr11:62646532-62646846 | Common:4; Rare:320; Clinvar (pathogenic):3 | ||||
| chr11:62653212-62653545 | Common:2; Rare:208 | ||||
| chr11:62665089-62665536 | Common:15; Rare:419 | ||||
| chr11:62671502-62672140 | Common:6; Rare:439; Clinvar (benign):8 | ||||
| chr11:62678924-62679277 | Rare:271 |