Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:44711335-44711640 | Rare:96; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr15:44711693-44711959 | Rare:46 | ||||
chr15:45023052-45023233 | Common:3; Rare:47 | ||||
chr15:45129905-45129996 | Rare:22 | ||||
chr15:45378444-45378687 | Common:4; Rare:69; Clinvar:2; Clinvar (benign):8 | ||||
chr15:45586989-45587263 | Common:1; Rare:55 | ||||
chr15:45587296-45587494 | Rare:64; Clinvar:6; Clinvar (benign):1 | ||||
chr15:48178128-48178274 | Common:1; Rare:55 | ||||
chr15:48331359-48331465 | Rare:37 | ||||
chr15:48645621-48645935 | Common:2; Rare:96; Clinvar (benign):1 | ||||
chr15:48878026-48878618 | Common:1; Rare:213 | ||||
chr15:49155530-49155878 | Common:2; Rare:113 | ||||
chr15:49170134-49170306 | Rare:40 | ||||
chr15:49423111-49423417 | Common:1; Rare:51 | ||||
chr15:49620794-49621099 | Common:6; Rare:123 |