Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:21286441-21286497 | Rare:10 | ||||
chr17:34254097-34254398 | Common:1; Rare:49 | ||||
chr17:40550747-40550921 | Common:2; Rare:20 | ||||
chr17:43315656-43315916 | Common:6; Rare:110 | ||||
chr17:50189694-50189862 | Common:3; Rare:39; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr17:50190070-50190331 | Common:1; Rare:81; Clinvar:3; Clinvar (benign):1 | ||||
chr17:58631834-58632132 | Common:3; Rare:125 | ||||
chr17:76557654-76557815 | Common:1; Rare:57 | ||||
chr18:3593940-3594099 | Common:2; Rare:26 | ||||
chr18:3603478-3603760 | Common:1; Rare:45 | ||||
chr18:3603996-3604214 | Rare:43 | ||||
chr18:5238006-5238130 | Common:1; Rare:49 | ||||
chr19:14622147-14622323 | Common:1; Rare:10 | ||||
chr19:27793219-27793479 | Common:4; Rare:60 | ||||
chr19:27793889-27794035 | Rare:32 |