Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:77319473-77319562 | Common:3; Rare:25; Clinvar (benign):3 | ||||
chr17:77319910-77319927 | Rare:6 | ||||
chr17:78186963-78187376 | Common:3; Rare:144 | ||||
chr17:78840742-78841035 | Common:2; Rare:106 | ||||
chr17:80035858-80036016 | Common:1; Rare:56 | ||||
chr17:80220330-80220447 | Rare:45; Clinvar:1 | ||||
chr17:81239029-81239373 | Common:4; Rare:111 | ||||
chr17:81512046-81512297 | Common:2; Rare:116; Clinvar:4; Clinvar (benign):14 | ||||
chr17:81512488-81512821 | Common:8; Rare:198; Clinvar (benign):15 | ||||
chr17:81666548-81666763 | Common:1; Rare:95 | ||||
chr17:81683680-81684052 | Common:4; Rare:189 | ||||
chr17:81703292-81703574 | Common:2; Rare:84; Clinvar (benign):2 | ||||
chr17:81855157-81855616 | Common:2; Rare:151 | ||||
chr17:81860324-81860358 | Rare:9 | ||||
chr17:81860386-81860627 | Common:1; Rare:109 |