Variant report

Variant	rs2099257
Chromosome Location	chr8:64423673-64423674
allele	C/T
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:32)

rs_ID	r²[population]
rs1019879	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10504364	0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1115753	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11775359	0.90[EUR][1000 genomes]
rs11775983	0.80[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12115114	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13255857	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs13280126	0.90[EUR][1000 genomes]
rs13280174	0.88[EUR][1000 genomes]
rs13280950	0.90[EUR][1000 genomes]
rs1367806	0.83[CEU][hapmap];1.00[CHB][hapmap];0.85[EUR][1000 genomes]
rs1367807	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1431585	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1897311	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1897312	0.91[CEU][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2116336	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2116337	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2116338	0.84[EUR][1000 genomes]
rs2195757	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2354895	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4531090	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4739097	0.80[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6472109	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6980849	0.80[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7012613	0.80[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7817045	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7820068	0.82[AMR][1000 genomes]
rs7823637	0.80[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7829623	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7831118	0.81[EUR][1000 genomes]
rs7836363	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs919620	0.93[CEU][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];0.81[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	nsv890967	chr8:64107847-64454446	Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 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	chr8:64409400-64428000	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr8:64409600-64428000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr8:64423400-64426600	Weak transcription	HUES64 Cell Line	embryonic stem cell

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