Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:16443351-16443683 | Common:3; Rare:74 | ||||
chr1:16499212-16499428 | Common:1; Rare:98 | ||||
chr1:16633200-16633321 | Common:2 | ||||
chr1:16644635-16644789 | Common:1; Rare:2 | ||||
chr1:16889383-16889511 | Common:3; Rare:24 | ||||
chr1:16895622-16895804 | Common:2; Rare:33 | ||||
chr1:16904813-16904950 | Common:2; Rare:17 | ||||
chr1:16911782-16911932 | Rare:25 | ||||
chr1:16913873-16914121 | Common:8; Rare:50 | ||||
chr1:17420723-17420903 | Common:1; Rare:39 | ||||
chr1:19328306-19328596 | Rare:67 | ||||
chr1:19656075-19656143 | Rare:13 | ||||
chr1:20483623-20483816 | Rare:41 | ||||
chr1:20654349-20654412 | Common:2; Rare:19; Clinvar (benign):2 | ||||
chr1:20655758-20655915 | Common:2; Rare:42; Clinvar (benign):1 |