Variant report

Variant	rs6772391
Chromosome Location	chr3:68775668-68775669
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11128088	0.82[EUR][1000 genomes]
rs13084200	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1504295	0.88[EUR][1000 genomes]
rs1504296	0.82[EUR][1000 genomes]
rs17047942	0.82[ASN][1000 genomes]
rs35132255	0.82[ASN][1000 genomes]
rs35586328	0.81[ASN][1000 genomes]
rs8180031	0.85[ASN][1000 genomes]
rs971381	0.81[EUR][1000 genomes]
rs9826485	0.82[EUR][1000 genomes]
rs9878555	0.82[EUR][1000 genomes]
rs9878718	0.82[EUR][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	nsv834722	chr3:68775036-68974120	Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:68775400-68776800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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

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