Variant report

Variant	rs6908194
Chromosome Location	chr6:70334305-70334306
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs2572991	0.80[EUR][1000 genomes]
rs2757758	0.80[EUR][1000 genomes]
rs34857559	0.96[EUR][1000 genomes]
rs4707218	0.96[EUR][1000 genomes]
rs6904921	1.00[CEU][hapmap];0.83[CHB][hapmap]
rs6915789	0.94[ASN][1000 genomes]
rs9346314	0.91[EUR][1000 genomes]
rs9351764	0.96[EUR][1000 genomes]
rs9364033	0.95[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	nsv1022847	chr6:70300521-70337899	Enhancers Bivalent Enhancer Weak transcription Active TSS	TF binding region Chromatin interactive region	3 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	chr6:70329400-70341400	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr6:70333800-70341000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr6:70334000-70335200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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