Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:46860822-46861133 | Common:3; Rare:100 | ||||
chr19:48966277-48966709 | Rare:144; Clinvar:1; Clinvar (pathogenic):2 | ||||
chr19:49104120-49104171 | Rare:19 | ||||
chr19:51594394-51594543 | Common:1; Rare:43 | ||||
chr19:51693125-51693328 | Common:3; Rare:42 | ||||
chr19:52601173-52601301 | Common:3; Rare:43 | ||||
chr19:52645079-52645325 | Common:1; Rare:40 | ||||
chr19:52923391-52923554 | Common:3; Rare:70 | ||||
chr19:52942540-52942782 | Common:8; Rare:89 | ||||
chr19:54207586-54207700 | Rare:32 | ||||
chr19:56765267-56765356 | Rare:22 | ||||
chr2:692827-693037 | Common:1; Rare:44 | ||||
chr2:693180-693400 | Rare:25 | ||||
chr2:740732-740897 | Common:7; Rare:34 | ||||
chr2:868290-868525 | Common:12; Rare:54 |