Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:2412474-2412851 | Common:2; Rare:160; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
chr1:2412940-2413132 | Rare:48 | ||||
chr1:2414262-2414315 | Rare:5 | ||||
chr1:2526117-2526454 | Common:2; Rare:114 | ||||
chr1:2526521-2526701 | Common:4; Rare:76 | ||||
chr1:2526881-2527033 | Rare:35 | ||||
chr1:2530261-2530280 | Rare:5 | ||||
chr1:2555664-2555860 | Common:2; Rare:60 | ||||
chr1:2555935-2556247 | Common:1; Rare:85 | ||||
chr1:2556288-2556673 | Common:2; Rare:149 | ||||
chr1:2556940-2557219 | Common:4; Rare:60 | ||||
chr1:2586348-2586500 | Common:1; Rare:41 | ||||
chr1:2586555-2586784 | Common:3; Rare:51 | ||||
chr1:3624696-3625075 | Common:1; Rare:117 | ||||
chr1:3649933-3650266 | Common:7; Rare:121 |