Variant report

Variant	rs7843537
Chromosome Location	chr8:49082018-49082019
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs11991972	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12114205	1.00[AMR][1000 genomes]
rs12114564	1.00[AMR][1000 genomes]
rs4304348	1.00[AMR][1000 genomes]
rs4546687	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4546688	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4609219	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4637865	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55708513	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55770276	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55956950	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56102090	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57688729	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57834756	1.00[AMR][1000 genomes]
rs58045776	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58175922	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58431112	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58555026	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59517761	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59634313	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60463191	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61602855	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73678239	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73678240	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73678243	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73678244	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73678245	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73678246	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73678259	1.00[AMR][1000 genomes]
rs7465660	1.00[AMR][1000 genomes];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	nsv931032	chr8:48744329-49091359	Strong transcription Flanking Active TSS Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv831310	chr8:49080177-49256440	Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv611307	chr8:49081709-49093889	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:49080200-49084600	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr8:49081600-49082400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived

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