Variant report

Variant	rs7279167
Chromosome Location	chr21:16874049-16874050
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs10854384	0.87[EUR][1000 genomes]
rs11088429	0.87[EUR][1000 genomes]
rs11911634	0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs55675962	0.86[EUR][1000 genomes]
rs62217396	0.85[EUR][1000 genomes]
rs62217397	0.87[EUR][1000 genomes]
rs62217398	0.87[EUR][1000 genomes]
rs62217399	0.87[EUR][1000 genomes]
rs7275233	0.86[EUR][1000 genomes]
rs7275540	0.86[EUR][1000 genomes]
rs7277561	0.86[EUR][1000 genomes]
rs7279689	0.89[EUR][1000 genomes]
rs7279999	0.89[CEU][hapmap];1.00[CHB][hapmap]
rs7282437	0.86[EUR][1000 genomes]
rs9305646	0.89[EUR][1000 genomes]

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	nsv1063385	chr21:16521617-16926212	Enhancers Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv1064280	chr21:16664312-17049272	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv834049	chr21:16717421-16905300	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv524022	chr21:16865946-16874741	Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:16871200-16874800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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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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