Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:171434718-171434824 | Rare:30 | ||||
chr2:171687982-171688048 | Rare:15 | ||||
chr2:171894210-171894334 | Rare:57; Clinvar:1 | ||||
chr2:171999831-171999972 | Common:1; Rare:58 | ||||
chr2:172427517-172427692 | Common:4; Rare:44; Clinvar:1; Clinvar (benign):1 | ||||
chr2:172821570-172821877 | Rare:43 | ||||
chr2:173075517-173075569 | Common:2; Rare:13 | ||||
chr2:173090551-173090746 | Rare:37 | ||||
chr2:173964091-173964309 | Rare:100 | ||||
chr2:173965245-173965513 | Common:1; Rare:93 | ||||
chr2:174248454-174248747 | Common:1; Rare:88 | ||||
chr2:174395623-174395799 | Common:2; Rare:57 | ||||
chr2:174486929-174487380 | Common:2; Rare:103 | ||||
chr2:175005135-175005311 | Rare:57; Clinvar:2 | ||||
chr2:175168105-175168558 | Common:2; Rare:121 |