Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:222589783-222589990 | Common:2; Rare:58 | ||||
chr1:222617849-222618143 | Common:3; Rare:76 | ||||
chr1:222644159-222644441 | Common:1; Rare:85 | ||||
chr1:222663789-222664005 | Rare:38 | ||||
chr1:222712434-222712881 | Common:3; Rare:153 | ||||
chr1:222713265-222713411 | Rare:46 | ||||
chr1:222739468-222739729 | Rare:52 | ||||
chr1:223143219-223143368 | Common:3; Rare:43 | ||||
chr1:224183097-224183401 | Common:3; Rare:120 | ||||
chr1:224330123-224330439 | Common:6; Rare:96 | ||||
chr1:224433683-224434064 | Common:1; Rare:115; Clinvar:1 | ||||
chr1:224434633-224434924 | Rare:83 | ||||
chr1:225427991-225428337 | Common:3; Rare:113; Clinvar:3; Clinvar (benign):2 | ||||
chr1:225777716-225777994 | Common:3; Rare:95 | ||||
chr1:225810578-225810607 | Rare:5 |