Variant report

Variant	rs3134697
Chromosome Location	chr6:55062324-55062325
allele	C/T
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]
rs3006851	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs3006855	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs3006856	1.00[AMR][1000 genomes]
rs3134688	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs3134695	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs3134702	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs3134709	1.00[AMR][1000 genomes]
rs9475139	1.00[AMR][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	nsv1016461	chr6:55038131-55129663	Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	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	chr6:55057800-55063200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr6:55060200-55063200	Weak transcription	Hela-S3	cervix
3	chr6:55062000-55062400	Enhancers	Stomach Mucosa	stomach

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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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