Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:15736246-15736355 | Common:1; Rare:17 | ||||
chr1:15736900-15736970 | Rare:7 | ||||
chr1:15756539-15756712 | Rare:48 | ||||
chr1:15757478-15757622 | Rare:20 | ||||
chr1:15757876-15757991 | Common:1; Rare:20 | ||||
chr1:15758464-15758777 | Rare:60 | ||||
chr1:16017934-16017962 | Rare:7 | ||||
chr1:16017986-16018059 | Common:1; Rare:30 | ||||
chr1:16352375-16352577 | Common:2; Rare:111 | ||||
chr1:16613336-16613373 | Common:1 | ||||
chr1:17053983-17054368 | Common:3; Rare:114; Clinvar:10; Clinvar (benign):9 | ||||
chr1:19210075-19210533 | Common:1; Rare:150 | ||||
chr1:19251496-19251838 | Common:6; Rare:115 | ||||
chr1:19288525-19288896 | Common:9; Rare:142 | ||||
chr1:19311961-19312350 | Common:8; Rare:174 |