Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:53196850-53197158 | Common:11; Rare:61 | ||||
chr19:53503723-53503903 | Common:1; Rare:22 | ||||
chr19:54137011-54137175 | Common:4; Rare:34 | ||||
chr19:57803766-57803893 | Rare:33 | ||||
chr2:3472970-3473050 | Rare:9 | ||||
chr2:13537616-13537689 | Rare:15 | ||||
chr2:19348006-19348092 | Common:1; Rare:37 | ||||
chr2:20447729-20447852 | Rare:33 | ||||
chr2:20447856-20448055 | Rare:64 | ||||
chr2:34992421-34992649 | Common:5; Rare:70 | ||||
chr2:36548281-36548562 | Common:1; Rare:82 | ||||
chr2:38481481-38481786 | Common:3; Rare:75 | ||||
chr2:46346708-46346999 | Rare:81; Clinvar:1 | ||||
chr2:46376251-46376590 | Common:5; Rare:100; Clinvar:1; Clinvar (benign):3 | ||||
chr2:47335212-47335323 | Rare:26 |