Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:200963465-200963930 | Common:1; Rare:117 | ||||
chr2:201071595-201072107 | Rare:115 | ||||
chr2:201115930-201116457 | Common:2; Rare:95 | ||||
chr2:201116682-201116822 | Rare:25 | ||||
chr2:201118744-201118857 | Rare:9 | ||||
chr2:201451417-201451821 | Common:2; Rare:109 | ||||
chr2:201642620-201642770 | Common:1; Rare:71; Clinvar (benign):1 | ||||
chr2:201780783-201780983 | Common:3; Rare:52; Clinvar:1; Clinvar (benign):2 | ||||
chr2:201781028-201781219 | Rare:52; Clinvar:2 | ||||
chr2:202034908-202035156 | Rare:69 | ||||
chr2:202238464-202238723 | Common:1; Rare:90; Clinvar:1 | ||||
chr2:202265633-202266022 | Common:2; Rare:148 | ||||
chr2:202634963-202635067 | Common:5; Rare:37 | ||||
chr2:202911463-202912048 | Common:1; Rare:131 | ||||
chr2:202912115-202912306 | Common:2; Rare:62 |