Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:77320077-77320329 | Common:1; Rare:66; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr17:78186985-78187364 | Common:3; Rare:130 | ||||
chr17:79009727-79009917 | Common:8; Rare:60; Clinvar:1; Clinvar (benign):1 | ||||
chr17:80220325-80220435 | Rare:46; Clinvar:1 | ||||
chr17:80415139-80415197 | Common:1; Rare:41 | ||||
chr17:80415428-80415492 | Common:3; Rare:25 | ||||
chr17:81239038-81239317 | Common:2; Rare:92 | ||||
chr17:81666548-81666783 | Common:1; Rare:107 | ||||
chr17:81683676-81684057 | Common:4; Rare:193 | ||||
chr17:81703286-81703489 | Common:2; Rare:55; Clinvar (benign):2 | ||||
chr17:81833243-81833371 | Rare:55 | ||||
chr17:81891605-81891848 | Common:1; Rare:115 | ||||
chr17:81937179-81937415 | Rare:81 | ||||
chr17:81977485-81977642 | Rare:53 | ||||
chr17:82037683-82037922 | Common:1; Rare:82 |