Variant report

Variant	rs11866447
Chromosome Location	chr16:52129218-52129219
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:16)

rs_ID	r²[population]
rs11863091	1.00[EUR][1000 genomes]
rs11864665	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11867065	1.00[EUR][1000 genomes]
rs13335560	1.00[EUR][1000 genomes]
rs1592493	1.00[EUR][1000 genomes]
rs16950945	1.00[EUR][1000 genomes]
rs16950957	1.00[EUR][1000 genomes]
rs28592818	1.00[EUR][1000 genomes]
rs28706188	1.00[EUR][1000 genomes]
rs4785069	1.00[EUR][1000 genomes]
rs60786559	1.00[EUR][1000 genomes]
rs7196724	1.00[EUR][1000 genomes]
rs74017250	1.00[EUR][1000 genomes]
rs74017271	1.00[EUR][1000 genomes]
rs74017272	1.00[EUR][1000 genomes]
rs74017273	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv492248	chr16:51681902-52456082	Enhancers Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
2	esv34024	chr16:51878565-52316530	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
3	nsv1058257	chr16:52093549-52271815	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	22 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	chr16:52128000-52129800	Enhancers	Fetal Kidney	kidney

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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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