Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:48233311-48233473 | Common:2; Rare:57 | ||||
chr13:48303657-48304021 | Common:1; Rare:123; Clinvar:13; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
chr13:48532643-48532940 | Common:4; Rare:106 | ||||
chr13:48533078-48533270 | Common:1; Rare:54 | ||||
chr13:48975786-48976112 | Common:1; Rare:108 | ||||
chr13:48976130-48976177 | Rare:17 | ||||
chr13:48976531-48976831 | Common:1; Rare:88 | ||||
chr13:49110216-49110402 | Common:2; Rare:58 | ||||
chr13:49247800-49247982 | Rare:51 | ||||
chr13:49443518-49443751 | Rare:32 | ||||
chr13:49443898-49444507 | Common:3; Rare:187 | ||||
chr13:49585491-49585669 | Common:1; Rare:64 | ||||
chr13:49792484-49792738 | Common:5; Rare:110 | ||||
chr13:49936234-49936608 | Common:2; Rare:112 | ||||
chr13:49996735-49997135 | Common:1; Rare:87 |