Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr12:121580241-121580384 | Rare:53 | ||||
chr12:122021822-122022025 | Common:9; Rare:57 | ||||
chr12:122266409-122266573 | Common:2; Rare:64 | ||||
chr12:122278925-122279137 | Common:1; Rare:51 | ||||
chr12:122422538-122422629 | Rare:27 | ||||
chr12:122526846-122527291 | Common:4; Rare:162 | ||||
chr12:122974580-122974843 | Rare:60 | ||||
chr12:123233077-123233496 | Common:3; Rare:143; Clinvar:1 | ||||
chr12:123364825-123364949 | Common:1; Rare:47 | ||||
chr12:123383770-123384205 | Rare:102 | ||||
chr12:123533712-123533720 | Rare:1 | ||||
chr12:123584295-123584611 | Common:6; Rare:106 | ||||
chr12:123584658-123584813 | Common:3; Rare:44 | ||||
chr12:123633547-123633855 | Common:1; Rare:147; Clinvar:8; Clinvar (benign):1 | ||||
chr12:123972535-123973329 | Common:8; Rare:258 |