Variant report

Variant	rs57906670
Chromosome Location	chr11:85054690-85054691
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs1016636	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10501591	1.00[ASN][1000 genomes]
rs1517315	1.00[ASN][1000 genomes]
rs1517316	1.00[ASN][1000 genomes]
rs17743080	1.00[ASN][1000 genomes]
rs17743269	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17743426	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17810494	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17810583	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2374650	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2888891	1.00[ASN][1000 genomes]
rs34821786	1.00[ASN][1000 genomes]
rs35119181	1.00[ASN][1000 genomes]
rs35439288	1.00[ASN][1000 genomes]
rs57325992	0.92[AFR][1000 genomes]
rs59376253	0.80[AFR][1000 genomes]
rs59420262	0.92[AFR][1000 genomes]
rs7105923	0.88[EUR][1000 genomes]
rs7116045	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7118453	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7127772	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7131233	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7936028	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7945053	0.88[EUR][1000 genomes]
rs7947168	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs876869	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1044370	chr11:84748993-85293233	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
2	nsv898043	chr11:84895033-85148689	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv898044	chr11:84895033-85220773	ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
4	nsv1051155	chr11:85006564-85721261	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
5	nsv541110	chr11:85006564-85721261	Enhancers Strong transcription Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 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	chr11:85049600-85059400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr11:85053000-85056600	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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