Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:62597201-62597545 | Common:1; Rare:60 | ||||
chr1:62688231-62688561 | Common:1; Rare:121; Clinvar:1 | ||||
chr1:63367479-63367686 | Rare:64; Clinvar (benign):1 | ||||
chr1:63523161-63523595 | Common:3; Rare:117 | ||||
chr1:63593106-63593465 | Rare:113; Clinvar (benign):1 | ||||
chr1:63594538-63594648 | Common:3; Rare:22 | ||||
chr1:63773910-63774104 | Rare:37 | ||||
chr1:64841243-64841604 | Rare:83; Clinvar:2 | ||||
chr1:65147313-65147670 | Rare:89 | ||||
chr1:65148721-65149068 | Common:3; Rare:101 | ||||
chr1:65420475-65420778 | Common:5; Rare:91; Clinvar:2; Clinvar (benign):1 | ||||
chr1:66533380-66533652 | Common:2; Rare:38 | ||||
chr1:66533869-66534173 | Common:2; Rare:76 | ||||
chr1:66752346-66752490 | Rare:29 | ||||
chr1:66924800-66925042 | Rare:101 |