Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:4806987-4807224 | Common:4; Rare:72 | ||||
chr17:4833302-4833639 | Common:1; Rare:79 | ||||
chr17:4899379-4899495 | Common:1; Rare:73; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr17:4939892-4940145 | Common:2; Rare:82 | ||||
chr17:4967755-4967983 | Rare:91 | ||||
chr17:4987640-4987726 | Rare:35 | ||||
chr17:4997900-4998063 | Common:1; Rare:62 | ||||
chr17:5191838-5192077 | Common:1; Rare:79 | ||||
chr17:5419646-5419863 | Common:3; Rare:65 | ||||
chr17:5420121-5420239 | Rare:49 | ||||
chr17:5486157-5486591 | Common:5; Rare:150 | ||||
chr17:6640651-6641066 | Common:7; Rare:123 | ||||
chr17:6651561-6651770 | Common:1; Rare:73 | ||||
chr17:6995811-6996062 | Common:1; Rare:53 | ||||
chr17:7012315-7012716 | Rare:134 |