Variant report

Variant	rs4869647
Chromosome Location	chr5:36333915-36333916
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs10461966	0.83[AMR][1000 genomes]
rs16902812	0.85[MEX][hapmap]
rs16902928	0.83[AMR][1000 genomes]
rs16902951	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2202006	0.83[AMR][1000 genomes]
rs4576170	0.83[AMR][1000 genomes]
rs57271540	0.80[ASN][1000 genomes]
rs72746423	0.80[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv881598	chr5:36248752-36382802	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:36333400-36334200	Enhancers	Colon Smooth Muscle	Colon
2	chr5:36333800-36334200	Enhancers	Rectal Smooth Muscle	rectum
3	chr5:36333800-36334800	Enhancers	Fetal Stomach	stomach

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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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