Variant report

Variant	rs848359
Chromosome Location	chr7:108540141-108540142
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs1624486	0.85[AMR][1000 genomes]
rs275548	0.85[AMR][1000 genomes]
rs275550	0.85[AMR][1000 genomes]
rs275551	0.85[AMR][1000 genomes]
rs848354	0.85[AMR][1000 genomes]
rs848355	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs848356	0.88[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs848357	0.88[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs848358	0.88[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs848371	1.00[AMR][1000 genomes]
rs848372	1.00[AMR][1000 genomes]
rs860229	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv817371	chr7:108199882-108649799	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	nsv1031096	chr7:108334543-108596014	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:108535000-108540600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
2	chr7:108535200-108540600	Weak transcription	HUES48 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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