Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:31722775-31722963 | Rare:48 | ||||
chr20:31819089-31819396 | Common:2; Rare:67 | ||||
chr20:32207686-32207944 | Common:3; Rare:100 | ||||
chr20:33401476-33401618 | Rare:37 | ||||
chr20:34112195-34112426 | Rare:67 | ||||
chr20:34516330-34516443 | Rare:41 | ||||
chr20:34558560-34558776 | Common:1; Rare:58 | ||||
chr20:34677086-34677329 | Rare:62 | ||||
chr20:34955744-34955928 | Common:1; Rare:69; Clinvar:2; Clinvar (benign):2 | ||||
chr20:35147302-35147416 | Rare:33 | ||||
chr20:35171846-35172119 | Rare:50 | ||||
chr20:35284728-35284817 | Common:1; Rare:32 | ||||
chr20:35455059-35455210 | Common:1; Rare:54 | ||||
chr20:35556712-35556993 | Common:2; Rare:70 | ||||
chr20:35664865-35664984 | Common:1; Rare:36 |