Variant report

Variant	rs7607326
Chromosome Location	chr2:167920834-167920835
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs16852932	1.00[CHB][hapmap]
rs16852940	1.00[CHB][hapmap]
rs6432967	0.83[TSI][hapmap]
rs6432982	0.82[CHB][hapmap]
rs6432983	0.82[CHB][hapmap]
rs6708222	1.00[GIH][hapmap];1.00[MEX][hapmap]
rs6738801	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs6740242	0.82[CHB][hapmap]
rs6741406	0.83[AMR][1000 genomes]
rs7423376	0.91[GIH][hapmap];1.00[MEX][hapmap];0.83[TSI][hapmap]
rs7565761	1.00[GIH][hapmap];1.00[MEX][hapmap]
rs7583143	1.00[GIH][hapmap];1.00[MEX][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529384	chr2:167143465-167958752	Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv875376	chr2:167844513-168037489	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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

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