Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:78840751-78841029 | Common:2; Rare:100 | ||||
chr17:79009732-79009924 | Common:8; Rare:57; Clinvar:1; Clinvar (benign):1 | ||||
chr17:80035867-80036025 | Common:1; Rare:51 | ||||
chr17:80220331-80220435 | Rare:40; Clinvar:1 | ||||
chr17:80415105-80415189 | Common:1; Rare:56 | ||||
chr17:80415384-80415492 | Common:4; Rare:41 | ||||
chr17:81666561-81666763 | Common:1; Rare:89 | ||||
chr17:81683621-81684057 | Common:5; Rare:234 | ||||
chr17:81703300-81703475 | Common:2; Rare:50; Clinvar (benign):2 | ||||
chr17:81891584-81891798 | Common:3; Rare:107 | ||||
chr17:81937179-81937415 | Rare:81 | ||||
chr17:82051578-82051934 | Common:2; Rare:113 | ||||
chr17:82273673-82273803 | Rare:37 | ||||
chr17:82458483-82458761 | Common:6; Rare:99 | ||||
chr18:267988-268238 | Common:1; Rare:87 |