Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:37218145-37218264 | Rare:19 | ||||
chr19:37317648-37317911 | Common:6; Rare:67 | ||||
chr19:37370911-37371202 | Common:5; Rare:63 | ||||
chr19:37467425-37467525 | Common:1; Rare:25 | ||||
chr19:37469273-37469405 | Common:2; Rare:38 | ||||
chr19:37594739-37594906 | Rare:47 | ||||
chr19:37655436-37655549 | Common:2; Rare:43 | ||||
chr19:37719728-37719869 | Rare:49 | ||||
chr19:37779583-37779694 | Rare:23 | ||||
chr19:37907045-37907289 | Rare:52 | ||||
chr19:38724308-38724562 | Common:2; Rare:90; Clinvar:1; Clinvar (benign):2 | ||||
chr19:38831768-38832043 | Common:4; Rare:80; Clinvar (benign):1 | ||||
chr19:38899537-38899998 | Rare:136 | ||||
chr19:38930738-38930992 | Common:3; Rare:68; Clinvar:2; Clinvar (benign):3 | ||||
chr19:39084055-39084371 | Common:1; Rare:80 |