Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:1013383-1013514 | Common:3; Rare:41 | ||||
chr1:1324598-1324900 | Common:3; Rare:151 | ||||
chr1:1399214-1399575 | Common:1; Rare:166 | ||||
chr1:1574541-1574997 | Common:1; Rare:214 | ||||
chr1:1615778-1615990 | Common:1; Rare:62 | ||||
chr1:1658923-1659290 | Common:6; Rare:143 | ||||
chr1:1692476-1692550 | Common:2; Rare:11 | ||||
chr1:1724273-1724460 | Common:3; Rare:66 | ||||
chr1:1890827-1891180 | Rare:126 | ||||
chr1:2391540-2391868 | Common:2; Rare:120 | ||||
chr1:3068864-3069254 | Common:3; Rare:94; Clinvar (benign):2 | ||||
chr1:3900219-3900347 | Common:10; Rare:66 | ||||
chr1:6199526-6199837 | Common:2; Rare:104 | ||||
chr1:6208680-6208886 | Common:1; Rare:58 | ||||
chr1:6485902-6486079 | Common:1; Rare:36 |