Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:39665293-39665412 | Common:1; Rare:34; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr17:39688010-39688094 | Rare:26 | ||||
chr17:39927492-39927745 | Common:2; Rare:74 | ||||
chr17:40121814-40121986 | Common:2; Rare:64 | ||||
chr17:40140177-40140562 | Common:5; Rare:191 | ||||
chr17:40342038-40342367 | Common:1; Rare:73 | ||||
chr17:41688661-41688897 | Common:1; Rare:78 | ||||
chr17:41812735-41813065 | Rare:84; Clinvar:5 | ||||
chr17:42017388-42017492 | Rare:45 | ||||
chr17:42423093-42423413 | Common:1; Rare:85; Clinvar:2 | ||||
chr17:42458738-42458936 | Common:3; Rare:75 | ||||
chr17:42577682-42577825 | Rare:64 | ||||
chr17:42609330-42609732 | Common:8; Rare:167; Clinvar (benign):2 | ||||
chr17:42760621-42760845 | Common:5; Rare:75 | ||||
chr17:42761024-42761264 | Rare:68 |