Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:18856189-18856380 | Common:1; Rare:35 | ||||
chr17:18857924-18858256 | Common:6; Rare:80 | ||||
chr17:19004149-19004336 | Rare:42 | ||||
chr17:19377638-19377788 | Common:2; Rare:41 | ||||
chr17:19377892-19378037 | Common:1; Rare:35 | ||||
chr17:19378156-19378581 | Common:2; Rare:100 | ||||
chr17:19387156-19387416 | Rare:65 | ||||
chr17:19648010-19648183 | Rare:38 | ||||
chr17:19648585-19649007 | Common:4; Rare:147; Clinvar (benign):1 | ||||
chr17:19977796-19977925 | Common:1; Rare:45 | ||||
chr17:19978074-19978194 | Common:1; Rare:23 | ||||
chr17:20009200-20009367 | Common:2; Rare:53 | ||||
chr17:20155847-20156121 | Common:1; Rare:89 | ||||
chr17:20868222-20868553 | Common:3; Rare:82 | ||||
chr17:20868631-20869074 | Common:3; Rare:107 |