Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:119206175-119206315 | Common:4; Rare:63; Clinvar:5; Clinvar (benign):3 | ||||
chr11:122864512-122864639 | Rare:28 | ||||
chr11:123062128-123062339 | Rare:76 | ||||
chr11:124622765-124622922 | Common:5; Rare:57 | ||||
chr11:124673709-124673942 | Common:4; Rare:70 | ||||
chr11:125592566-125592885 | Common:6; Rare:104 | ||||
chr11:126211638-126211806 | Rare:77 | ||||
chr11:126268812-126269199 | Common:1; Rare:150; Clinvar:2; Clinvar (benign):3 | ||||
chr11:126270249-126270500 | Common:4; Rare:30 | ||||
chr11:126283487-126283626 | Rare:26 | ||||
chr11:126303989-126304108 | Rare:72 | ||||
chr11:128693740-128694266 | Common:3; Rare:107 | ||||
chr11:130189818-130190115 | Common:2; Rare:105; Clinvar:1 | ||||
chr11:134253314-134253576 | Common:2; Rare:85; Clinvar (benign):1 | ||||
chr12:389242-389391 | Common:1; Rare:55 |