Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:181090428-181090495 | Rare:10 | ||||
chr1:181148992-181149273 | Common:3; Rare:34 | ||||
chr1:181152953-181153116 | Common:1; Rare:40 | ||||
chr1:197201238-197201523 | Common:1; Rare:96 | ||||
chr1:201358756-201359058 | Common:3; Rare:64 | ||||
chr1:201359584-201359685 | Common:1; Rare:27; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
chr1:201374593-201374859 | Common:1; Rare:36 | ||||
chr1:202495289-202495679 | Common:1; Rare:105 | ||||
chr1:203629981-203630070 | Common:1; Rare:9 | ||||
chr1:204410111-204410384 | Common:1; Rare:74 | ||||
chr1:206664897-206665149 | Common:4; Rare:38 | ||||
chr1:207822700-207822908 | Common:1; Rare:41 | ||||
chr1:211382727-211382849 | Common:1; Rare:49 | ||||
chr1:218345200-218345346 | Rare:28 | ||||
chr1:223992564-223992818 | Common:4; Rare:91 |