Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:75979100-75979312 | Rare:60; Clinvar:4 | ||||
chr17:75979374-75979464 | Common:1; Rare:26; Clinvar (benign):1 | ||||
chr17:76537682-76537957 | Common:1; Rare:66 | ||||
chr17:76726464-76727151 | Common:7; Rare:276 | ||||
chr17:76737325-76737537 | Common:2; Rare:81 | ||||
chr17:77319434-77319561 | Common:3; Rare:33; Clinvar (benign):3 | ||||
chr17:77451262-77451441 | Rare:43 | ||||
chr17:78186988-78187364 | Common:3; Rare:130 | ||||
chr17:78840736-78841060 | Common:2; Rare:118 | ||||
chr17:79009717-79009935 | Common:9; Rare:65; Clinvar:2; Clinvar (benign):1 | ||||
chr17:80035852-80036030 | Common:1; Rare:62 | ||||
chr17:80220370-80220447 | Rare:25 | ||||
chr17:80415397-80415500 | Common:4; Rare:41 | ||||
chr17:81239038-81239381 | Common:4; Rare:111 | ||||
chr17:81636931-81637246 | Common:3; Rare:127 |