Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:25232460-25232655 | Rare:75 | ||||
chr1:25819855-25820208 | Common:5; Rare:107 | ||||
chr1:26432123-26432428 | Common:4; Rare:81; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26695608-26695803 | Rare:64 | ||||
chr1:27366942-27367016 | Rare:11 | ||||
chr1:28505847-28506084 | Common:2; Rare:109 | ||||
chr1:28643024-28643181 | Rare:62 | ||||
chr1:31296720-31297082 | Common:5; Rare:125 | ||||
chr1:31577893-31578189 | Rare:47 | ||||
chr1:32650922-32651307 | Common:2; Rare:149 | ||||
chr1:32817261-32817686 | Rare:115; Clinvar:5; Clinvar (benign):1 | ||||
chr1:34985303-34985370 | Common:1; Rare:23 | ||||
chr1:35031663-35032008 | Common:1; Rare:99 | ||||
chr1:35079314-35079386 | Common:1; Rare:21 | ||||
chr1:35193099-35193312 | Rare:79 |