Variant report

Variant	rs73480536
Chromosome Location	chr6:82493893-82493894
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs16893522	0.89[ASN][1000 genomes]
rs73480512	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs73480533	1.00[AMR][1000 genomes]
rs73480546	1.00[AMR][1000 genomes]
rs9449366	0.92[ASN][1000 genomes]
rs9449367	0.92[ASN][1000 genomes]
rs9449368	0.92[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	nsv830712	chr6:82491029-82654531	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:82483000-82497400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:82491800-82494800	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr6:82492000-82498400	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr6:82493400-82494000	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr6:82493800-82494000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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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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