Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:39955004-39955170 | Common:1; Rare:43 | ||||
chr1:40039884-40040061 | Common:2; Rare:42 | ||||
chr1:40040444-40040812 | Common:3; Rare:114 | ||||
chr1:40161265-40161399 | Rare:36 | ||||
chr1:40257903-40258313 | Common:4; Rare:113; Clinvar:7; Clinvar (benign):1 | ||||
chr1:40508626-40508769 | Common:5; Rare:43 | ||||
chr1:40691572-40691805 | Common:1; Rare:116 | ||||
chr1:40692033-40692278 | Common:1; Rare:81 | ||||
chr1:40979394-40979739 | Common:4; Rare:109 | ||||
chr1:41242105-41242383 | Rare:80 | ||||
chr1:42335149-42335395 | Common:5; Rare:121 | ||||
chr1:42456007-42456381 | Common:1; Rare:98 | ||||
chr1:42456488-42456590 | Rare:54 | ||||
chr1:42658285-42658463 | Common:2; Rare:52 | ||||
chr1:42682175-42682448 | Common:2; Rare:66 |