Variant report

Variant	rs370425634
Chromosome Location	chr3:118281542-118281543
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv829690	chr3:118205361-118378010	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	esv3441762	chr3:118280912-118282860	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	inside rSNPs	diseases
3	esv3373228	chr3:118281412-118282360	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	inside rSNPs	diseases
4	esv1969233	chr3:118281424-118282003	Weak transcription Strong transcription	n/a	n/a	inside rSNPs	diseases
5	esv3519907	chr3:118281508-118281939	Weak transcription Strong transcription	n/a	n/a	inside rSNPs	diseases
6	esv3365184	chr3:118281511-118281925	Weak transcription Strong transcription	n/a	n/a	inside rSNPs	diseases
7	esv3519909	chr3:118281516-118281900	Weak transcription Strong transcription	n/a	n/a	inside rSNPs	diseases
8	esv3519906	chr3:118281520-118281862	Weak transcription Strong transcription	n/a	n/a	inside rSNPs	diseases
9	esv3462388	chr3:118281529-118281902	Strong transcription Weak transcription	n/a	n/a	inside rSNPs	diseases
10	esv3462387	chr3:118281532-118281904	Weak transcription Strong transcription	n/a	n/a	inside rSNPs	diseases
11	esv3462389	chr3:118281542-118281853	Weak transcription Strong transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:118268000-118305800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr3:118271800-118291200	Weak transcription	Pancreas	Pancrea
3	chr3:118280000-118282600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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