Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr12:121513840-121514016 | Rare:35 | ||||
chr12:121846913-121847115 | Rare:57; Clinvar:1; Clinvar (benign):1 | ||||
chr12:121931610-121931854 | Rare:66 | ||||
chr12:122126800-122127061 | Common:1; Rare:43 | ||||
chr12:124821711-124822061 | Common:2; Rare:59 | ||||
chr12:124828696-124828945 | Common:2; Rare:40 | ||||
chr12:124831719-124831859 | Common:1; Rare:32 | ||||
chr12:125983363-125983704 | Common:10; Rare:89 | ||||
chr12:127060359-127060617 | Common:4; Rare:85 | ||||
chr12:127146078-127146233 | Rare:73 | ||||
chr12:132605138-132605447 | Common:3; Rare:50 | ||||
chr13:21298030-21298201 | Common:3; Rare:46 | ||||
chr13:23888780-23888872 | Common:1; Rare:26 | ||||
chr13:24183816-24184027 | Rare:42 | ||||
chr13:27212662-27212700 | Rare:8 |