Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:75979088-75979283 | Rare:53; Clinvar:4 | ||||
chr17:75979388-75979481 | Common:1; Rare:25; Clinvar (benign):1 | ||||
chr17:76072497-76072636 | Rare:41 | ||||
chr17:76103646-76103867 | Common:6; Rare:76 | ||||
chr17:76726467-76726893 | Common:5; Rare:163 | ||||
chr17:76737328-76737525 | Common:2; Rare:73 | ||||
chr17:76737892-76738062 | Common:3; Rare:49 | ||||
chr17:77450316-77450556 | Common:1; Rare:51 | ||||
chr17:78187052-78187371 | Common:3; Rare:100 | ||||
chr17:78378594-78378706 | Common:1; Rare:48 | ||||
chr17:78723556-78723660 | Rare:29 | ||||
chr17:78782255-78782583 | Common:9; Rare:107 | ||||
chr17:78840745-78841029 | Common:2; Rare:102 | ||||
chr17:79009742-79009924 | Common:8; Rare:53; Clinvar:1; Clinvar (benign):1 | ||||
chr17:80035843-80035983 | Common:1; Rare:52 |