Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:77453949-77454039 | Common:1; Rare:20 | ||||
chr17:78125231-78125477 | Common:1; Rare:61; Clinvar:1; Clinvar (benign):1 | ||||
chr17:78130574-78130796 | Rare:44 | ||||
chr17:78187045-78187364 | Common:3; Rare:100 | ||||
chr17:78840735-78841037 | Common:2; Rare:110 | ||||
chr17:79009732-79009924 | Common:8; Rare:57; Clinvar:1; Clinvar (benign):1 | ||||
chr17:80220325-80220435 | Rare:46; Clinvar:1 | ||||
chr17:80415126-80415189 | Common:1; Rare:42 | ||||
chr17:81512735-81513155 | Common:7; Rare:209; Clinvar (benign):14 | ||||
chr17:81553120-81553366 | Common:1; Rare:54 | ||||
chr17:81666554-81666758 | Common:1; Rare:87 | ||||
chr17:81683720-81684052 | Common:4; Rare:165 | ||||
chr17:81703283-81703510 | Common:2; Rare:65; Clinvar (benign):2 | ||||
chr17:81833248-81833332 | Rare:37 | ||||
chr17:81977485-81977642 | Rare:53 |