Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:83861003-83861118 | Rare:28 | ||||
chr1:94864116-94864228 | Rare:20 | ||||
chr1:155247796-155248192 | Common:1; Rare:127 | ||||
chr1:155257312-155257532 | Rare:71 | ||||
chr1:183630631-183630930 | Common:1; Rare:61 | ||||
chr1:201874908-201875178 | Common:3; Rare:67 | ||||
chr1:202861524-202861785 | Common:1; Rare:73 | ||||
chr1:209883331-209883566 | Common:2; Rare:47 | ||||
chr1:226542726-226542958 | Common:1; Rare:36 | ||||
chr1:226703486-226703639 | Common:1; Rare:58 | ||||
chr1:230236396-230236689 | Rare:71 | ||||
chr1:231422236-231422430 | Common:4; Rare:88; Clinvar:4; Clinvar (benign):5 | ||||
chr1:235882194-235882251 | Rare:9 | ||||
chr1:235908965-235909106 | Rare:22 | ||||
chr1:244863616-244863955 | Rare:120; Clinvar:6; Clinvar (benign):5; Clinvar (pathogenic):1 |