Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:32315435-32315582 | Rare:43; Clinvar:2; Clinvar (benign):2 | ||||
chr13:32538737-32538973 | Common:1; Rare:58 | ||||
chr13:32586236-32586582 | Common:2; Rare:103 | ||||
chr13:33285677-33285904 | Rare:50 | ||||
chr13:33350625-33350737 | Rare:29 | ||||
chr13:36345546-36345658 | Common:1; Rare:22 | ||||
chr13:36346249-36346478 | Common:3; Rare:63; Clinvar:2; Clinvar (benign):2 | ||||
chr13:36999265-36999465 | Rare:80 | ||||
chr13:37000248-37000404 | Common:2; Rare:30 | ||||
chr13:37000574-37000815 | Common:1; Rare:81; Clinvar (pathogenic):1 | ||||
chr13:38349536-38349911 | Common:4; Rare:124; Clinvar (pathogenic):1 | ||||
chr13:39038064-39038433 | Common:1; Rare:92 | ||||
chr13:40771041-40771440 | Common:3; Rare:129 | ||||
chr13:40789385-40789615 | Common:2; Rare:76; Clinvar:5; Clinvar (benign):2 | ||||
chr13:41061356-41061649 | Common:2; Rare:90 |