Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:85593786-85594098 | Common:1; Rare:89 | ||||
chr6:85643817-85643946 | Common:2; Rare:40 | ||||
chr6:87155280-87155601 | Rare:87 | ||||
chr6:87589925-87590163 | Common:2; Rare:116; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr6:88963599-88963830 | Common:2; Rare:77 | ||||
chr6:89081048-89081335 | Rare:116 | ||||
chr6:89638438-89638552 | Common:1; Rare:23 | ||||
chr6:89638721-89638799 | Common:1; Rare:28 | ||||
chr6:89829620-89829909 | Rare:68 | ||||
chr6:95577404-95577543 | Common:3; Rare:37 | ||||
chr6:96521723-96521875 | Common:3; Rare:72 | ||||
chr6:96897821-96898073 | Common:4; Rare:92; Clinvar:3; Clinvar (benign):1 | ||||
chr6:99425259-99425422 | Common:1; Rare:47 | ||||
chr6:100881245-100881460 | Common:4; Rare:82 | ||||
chr6:106325620-106325957 | Common:1; Rare:122 |