Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:30906707-30906731 | Rare:11 | ||||
chr13:32253948-32254329 | Common:3; Rare:80 | ||||
chr13:33285666-33285900 | Rare:54 | ||||
chr13:35476308-35476611 | Rare:55 | ||||
chr13:35476647-35476822 | Common:1; Rare:29 | ||||
chr13:36346044-36346239 | Common:1; Rare:43; Clinvar (benign):1 | ||||
chr13:36346258-36346477 | Common:3; Rare:61; Clinvar:2; Clinvar (benign):2 | ||||
chr13:37000532-37000805 | Common:3; Rare:87 | ||||
chr13:37059600-37059726 | Common:1; Rare:45 | ||||
chr13:38350239-38350373 | Rare:43 | ||||
chr13:39038081-39038484 | Common:1; Rare:98 | ||||
chr13:39603114-39603444 | Common:2; Rare:117 | ||||
chr13:40771155-40771333 | Common:3; Rare:49 | ||||
chr13:40982862-40983035 | Common:3; Rare:28 | ||||
chr13:41060868-41061058 | Common:16; Rare:111 |