Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:214551554-214551824 | Rare:88 | ||||
chr1:217078222-217078572 | Common:1; Rare:53 | ||||
chr1:217630954-217631385 | Common:4; Rare:128 | ||||
chr1:219173766-219173893 | Common:1; Rare:68 | ||||
chr1:221741993-221742438 | Common:2; Rare:108 | ||||
chr1:222589781-222589994 | Common:2; Rare:58 | ||||
chr1:222617849-222618119 | Common:3; Rare:67 | ||||
chr1:222644109-222644397 | Common:2; Rare:85 | ||||
chr1:222712437-222712864 | Common:3; Rare:149 | ||||
chr1:222713234-222713411 | Common:1; Rare:55 | ||||
chr1:223143196-223143358 | Common:3; Rare:50 | ||||
chr1:224183038-224183316 | Common:3; Rare:114 | ||||
chr1:224330131-224330438 | Common:6; Rare:93 | ||||
chr1:224434792-224434924 | Rare:32 | ||||
chr1:225427994-225428239 | Common:3; Rare:73; Clinvar:3; Clinvar (benign):2 |