Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:46722188-46722213 | Rare:6 | ||||
chr17:58332513-58332807 | Common:3; Rare:71 | ||||
chr17:58337250-58337372 | Rare:23 | ||||
chr17:62065926-62066175 | Common:1; Rare:81 | ||||
chr17:63931350-63931492 | Rare:43; Clinvar (benign):1 | ||||
chr17:64145743-64145975 | Common:2; Rare:62 | ||||
chr17:64837112-64837328 | Common:1; Rare:62 | ||||
chr17:64966037-64966268 | Common:1; Rare:59 | ||||
chr17:64985905-64986179 | Rare:57 | ||||
chr17:65100704-65100896 | Rare:57 | ||||
chr17:66781209-66781360 | Rare:28 | ||||
chr17:67813253-67813523 | Common:2; Rare:54 | ||||
chr17:68101481-68101566 | Common:3; Rare:44 | ||||
chr17:69500922-69501063 | Rare:14 | ||||
chr17:69516950-69517185 | Rare:34 |