Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:124917071-124917268 | Rare:65 | ||||
chr10:124983174-124983512 | Common:1; Rare:70 | ||||
chr10:125903113-125903423 | Common:2; Rare:18 | ||||
chr10:126631494-126631815 | Common:2; Rare:61 | ||||
chr10:126910340-126910405 | Rare:8 | ||||
chr10:130110456-130110581 | Common:2; Rare:43 | ||||
chr10:130110812-130110890 | Rare:24 | ||||
chr10:131970883-131971122 | Rare:61 | ||||
chr10:131973195-131973414 | Rare:50 | ||||
chr10:133498809-133499135 | Common:3; Rare:47 | ||||
chr11:383661-383810 | Common:2; Rare:19 | ||||
chr11:653817-654022 | Common:1; Rare:68; Clinvar:2; Clinvar (benign):1 | ||||
chr11:763039-763410 | Common:24; Rare:177; Clinvar:2; Clinvar (pathogenic):1 | ||||
chr11:812846-813029 | Rare:47 | ||||
chr11:840479-840550 | Rare:29 |