Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:79537309-79537665 | Common:2; Rare:110; Clinvar:5 | ||||
chr6:79630960-79631358 | Common:2; Rare:79 | ||||
chr6:80106434-80106690 | Common:1; Rare:80 | ||||
chr6:81752644-81752821 | Rare:93 | ||||
chr6:83193222-83193414 | Common:3; Rare:70 | ||||
chr6:84764550-84764773 | Rare:63 | ||||
chr6:85449905-85450277 | Common:1; Rare:110 | ||||
chr6:85643810-85643874 | Rare:23 | ||||
chr6:87155240-87155620 | Rare:107 | ||||
chr6:87472900-87473004 | Common:1; Rare:40; Clinvar (benign):4 | ||||
chr6:87589955-87590165 | Common:2; Rare:93; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr6:88963579-88963869 | Common:2; Rare:101 | ||||
chr6:89081049-89081340 | Rare:117 | ||||
chr6:89145983-89146090 | Rare:32 | ||||
chr6:89412072-89412395 | Common:3; Rare:77 |