Variant report

Variant	rs7617224
Chromosome Location	chr3:139913460-139913461
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs1564396	1.00[MEX][hapmap]
rs16849957	1.00[MEX][hapmap]
rs16849961	1.00[MEX][hapmap]
rs16849965	1.00[MEX][hapmap]
rs16849992	1.00[MEX][hapmap]
rs16850037	1.00[AMR][1000 genomes]
rs57732985	1.00[AMR][1000 genomes]
rs58104749	1.00[AMR][1000 genomes]
rs61464238	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6439901	1.00[MEX][hapmap];1.00[AMR][1000 genomes]
rs6786062	1.00[MEX][hapmap]
rs6787416	1.00[AMR][1000 genomes]
rs7615973	1.00[AMR][1000 genomes]
rs7618174	1.00[MEX][hapmap]
rs7618652	1.00[AMR][1000 genomes]
rs7630704	1.00[MEX][hapmap]
rs7637809	1.00[AMR][1000 genomes]
rs7650468	1.00[AMR][1000 genomes]
rs922565	1.00[MEX][hapmap]
rs9826117	1.00[AMR][1000 genomes]
rs9828897	1.00[MEX][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv998423	chr3:139526446-139947336	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv829739	chr3:139797496-140002685	Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv1008578	chr3:139907172-139942453	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv1003141	chr3:139907434-139942453	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region	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	chr3:139901600-139915000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr3:139909200-139917000	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr3:139913200-139913600	Weak transcription	HSMMtube	muscle

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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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