| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:62591434-62591965 | Rare:180 | ||||
| chr11:62592088-62592143 | Rare:6 | ||||
| chr11:62592149-62592170 | Rare:3 | ||||
| chr11:62600020-62600208 | Common:1; Rare:38 | ||||
| chr11:62601190-62601341 | Rare:36 | ||||
| chr11:62601601-62602210 | Common:2; Rare:171 | ||||
| chr11:62612355-62612879 | Common:5; Rare:155; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:62613065-62613185 | Rare:37; Clinvar:1 | ||||
| chr11:62621726-62621863 | Rare:42 | ||||
| chr11:62621881-62622359 | Common:4; Rare:144 | ||||
| chr11:62646537-62646817 | Common:1; Rare:116; Clinvar (pathogenic):1 | ||||
| chr11:62653160-62653559 | Common:1; Rare:108 | ||||
| chr11:62664722-62664762 | Rare:4 | ||||
| chr11:62664769-62664939 | Common:1; Rare:57 | ||||
| chr11:62665112-62665343 | Common:4; Rare:108 |