Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:42773314-42773484 | Rare:46 | ||||
chr17:42833385-42833491 | Rare:46 | ||||
chr17:42964436-42964536 | Rare:48 | ||||
chr17:42998303-42998547 | Common:4; Rare:74 | ||||
chr17:43125338-43125654 | Rare:80; Clinvar:3; Clinvar (benign):2 | ||||
chr17:43170205-43170502 | Common:2; Rare:67 | ||||
chr17:43170885-43171255 | Rare:119 | ||||
chr17:43483661-43484038 | Rare:104 | ||||
chr17:43546340-43546616 | Common:1; Rare:67 | ||||
chr17:44070636-44070951 | Common:3; Rare:114; Clinvar:4; Clinvar (benign):2 | ||||
chr17:44141784-44141945 | Common:1; Rare:33 | ||||
chr17:44186672-44186998 | Common:1; Rare:116 | ||||
chr17:44198420-44198851 | Common:2; Rare:121 | ||||
chr17:44324769-44324963 | Common:2; Rare:68 | ||||
chr17:44350795-44351117 | Rare:104; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):3 |