Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:85643817-85643946 | Common:2; Rare:40 | ||||
chr6:87155292-87155588 | Rare:79 | ||||
chr6:87472892-87472997 | Common:1; Rare:40; Clinvar (benign):4 | ||||
chr6:87589946-87590165 | Common:2; Rare:100; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr6:87702228-87702474 | Common:1; Rare:70 | ||||
chr6:88963545-88963645 | Rare:26 | ||||
chr6:89352699-89353007 | Common:1; Rare:68 | ||||
chr6:89638434-89638549 | Common:1; Rare:25 | ||||
chr6:89638721-89638845 | Common:3; Rare:42 | ||||
chr6:89819732-89819863 | Rare:47 | ||||
chr6:89829614-89829909 | Rare:69 | ||||
chr6:90587037-90587266 | Common:2; Rare:58 | ||||
chr6:93419557-93419824 | Common:1; Rare:71 | ||||
chr6:95577404-95577597 | Common:5; Rare:56 | ||||
chr6:96521671-96521866 | Common:8; Rare:94 |