Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:196260019-196260166 | Common:1; Rare:32 | ||||
chr2:197487876-197488214 | Rare:87; Clinvar:2; Clinvar (benign):3 | ||||
chr2:197495342-197495575 | Common:3; Rare:47; Clinvar:2; Clinvar (benign):1 | ||||
chr2:200467210-200467356 | Rare:28 | ||||
chr2:201124219-201124447 | Common:1; Rare:29 | ||||
chr2:201126671-201127002 | Rare:44 | ||||
chr2:201127654-201127683 | Rare:3 | ||||
chr2:201151238-201151399 | Rare:27 | ||||
chr2:201157728-201157977 | Common:1; Rare:48 | ||||
chr2:201158160-201158335 | Common:1; Rare:33 | ||||
chr2:201420585-201420848 | Rare:35 | ||||
chr2:202375528-202375870 | Common:1; Rare:74 | ||||
chr2:202376105-202376245 | Rare:76 | ||||
chr2:203454444-203454653 | Rare:54 | ||||
chr2:206084358-206084664 | Common:1; Rare:65 |