Variant report

Variant	rs16997277
Chromosome Location	chr20:16152468-16152469
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs11696962	0.89[ASN][1000 genomes]
rs11697305	0.91[EUR][1000 genomes]
rs11697341	0.91[EUR][1000 genomes]
rs11697461	0.89[ASN][1000 genomes]
rs11698180	0.89[ASN][1000 genomes]
rs11698334	0.91[EUR][1000 genomes]
rs11698862	0.89[ASN][1000 genomes]
rs11907241	1.00[JPT][hapmap]
rs17648202	0.89[ASN][1000 genomes]
rs17655074	0.91[EUR][1000 genomes]
rs17655092	0.88[EUR][1000 genomes]
rs17727461	0.89[ASN][1000 genomes]
rs17728209	0.96[EUR][1000 genomes]
rs17728269	0.91[EUR][1000 genomes]
rs36085973	0.91[EUR][1000 genomes]
rs4416282	1.00[JPT][hapmap]
rs6111004	1.00[JPT][hapmap]
rs6111005	1.00[JPT][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	nsv869328	chr20:15325423-16213898	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv1059778	chr20:15999519-16165895	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv544207	chr20:15999519-16165895	Weak transcription Bivalent Enhancer Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv833930	chr20:16134347-16302763	Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	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	chr20:16150800-16152800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood

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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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