Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr12:31651980-31652199 | Common:3; Rare:91 | ||||
chr12:45727488-45727715 | Rare:164 | ||||
chr12:45727740-45728300 | Common:5; Rare:181 | ||||
chr12:45730784-45731054 | Common:2; Rare:49 | ||||
chr12:45989589-45989932 | Common:2; Rare:82 | ||||
chr12:46373699-46374140 | Common:2; Rare:173 | ||||
chr12:46383313-46383716 | Common:5; Rare:231 | ||||
chr12:46383740-46384120 | Common:3; Rare:179 | ||||
chr12:46384613-46385060 | Common:3; Rare:152 | ||||
chr12:46492451-46493051 | Common:4; Rare:173 | ||||
chr12:46524151-46524651 | Common:4; Rare:166 | ||||
chr12:47910060-47910510 | Common:4; Rare:77 | ||||
chr12:47999741-48000400 | Common:4; Rare:209; Clinvar:2; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
chr12:48940974-48941451 | Common:6; Rare:149 | ||||
chr12:49060519-49060907 | Common:2; Rare:240 |