Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:35438158-35438226 | Common:1; Rare:13; Clinvar (benign):1 | ||||
chr20:35542350-35542472 | Rare:36 | ||||
chr20:35699321-35699429 | Rare:33; Clinvar (benign):2 | ||||
chr20:36236408-36236493 | Common:1; Rare:18 | ||||
chr20:37289534-37289672 | Common:1; Rare:39 | ||||
chr20:38033421-38033789 | Common:2; Rare:106 | ||||
chr20:38962158-38962382 | Common:1; Rare:94 | ||||
chr20:44210624-44211106 | Common:5; Rare:170 | ||||
chr20:44651650-44651822 | Common:1; Rare:51; Clinvar (benign):1 | ||||
chr20:45791884-45791989 | Rare:38 | ||||
chr20:45857326-45857617 | Common:3; Rare:78 | ||||
chr20:45891204-45891425 | Common:1; Rare:66; Clinvar:3; Clinvar (benign):1 | ||||
chr20:45910904-45911214 | Common:4; Rare:98 | ||||
chr20:45934644-45934727 | Rare:40 | ||||
chr20:45935051-45935354 | Rare:117 |