Variant report

Variant	rs7843208
Chromosome Location	chr8:110679137-110679138
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs10092211	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10092626	1.00[CEU][hapmap]
rs10096439	1.00[CEU][hapmap]
rs10098728	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10105594	1.00[CEU][hapmap]
rs10105602	1.00[CEU][hapmap]
rs10106169	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10106568	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10106809	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10107091	1.00[CEU][hapmap];0.87[AMR][1000 genomes]
rs11988264	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs16879807	1.00[CEU][hapmap]
rs16879840	1.00[CEU][hapmap]
rs16879862	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs16879869	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs16879889	0.81[ASN][1000 genomes]
rs16879903	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs16879906	0.81[ASN][1000 genomes]
rs28404625	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs28465493	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs28636990	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs28637942	0.87[AMR][1000 genomes]
rs28726128	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4313130	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs4506181	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs56384256	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs56838167	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57167766	0.81[ASN][1000 genomes]
rs57285880	0.81[ASN][1000 genomes]
rs58404081	0.81[ASN][1000 genomes]
rs58910462	0.81[ASN][1000 genomes]
rs59161508	0.81[ASN][1000 genomes]
rs59892422	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs59981669	1.00[ASN][1000 genomes]
rs60841208	0.81[ASN][1000 genomes]
rs61437630	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs61702273	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6469277	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6987830	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7011702	1.00[EUR][1000 genomes]
rs7017357	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs73321006	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs73321029	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7817360	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7817773	0.81[ASN][1000 genomes]
rs7824472	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7825942	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7841022	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7842227	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9297431	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9774677	1.00[CEU][hapmap]

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	esv1849702	chr8:110594148-110683804	Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 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	chr8:110672000-110680200	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr8:110678200-110679200	Enhancers	Stomach Smooth Muscle	stomach
3	chr8:110678800-110679800	Weak transcription	Fetal Brain Male	brain

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