Variant report

Variant	rs6435664
Chromosome Location	chr2:212585065-212585066
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs12162287	0.86[CEU][hapmap];0.86[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.91[MKK][hapmap];0.97[TSI][hapmap];0.89[AFR][1000 genomes];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs13002712	0.82[CHB][hapmap];0.93[CHD][hapmap];0.80[GIH][hapmap];0.86[JPT][hapmap];1.00[YRI][hapmap];0.85[ASN][1000 genomes]
rs13393587	0.86[CEU][hapmap];0.86[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap];0.89[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs13411267	0.87[EUR][1000 genomes]
rs6435667	1.00[YRI][hapmap]
rs6758063	0.83[TSI][hapmap]
rs7419310	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7421820	0.80[MEX][hapmap];1.00[YRI][hapmap]
rs7422904	0.87[EUR][1000 genomes]
rs7422905	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7425190	0.86[CEU][hapmap];0.87[EUR][1000 genomes]
rs7425201	0.87[EUR][1000 genomes]
rs7563762	0.90[EUR][1000 genomes]
rs7604206	0.95[CEU][hapmap];0.90[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	esv34128	chr2:212581485-212857122	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:212569400-212590800	Weak transcription	Fetal Kidney	kidney
2	chr2:212569600-212591800	Weak transcription	Fetal Heart	heart
3	chr2:212571200-212594800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr2:212575600-212592000	Weak transcription	Aorta	Aorta
5	chr2:212582800-212587400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr2:212583600-212589800	Weak transcription	Left Ventricle	heart
7	chr2:212583600-212595400	Weak transcription	Brain Anterior Caudate	brain
8	chr2:212585000-212587400	Weak transcription	Right Ventricle	heart

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Input of quick search could be:

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

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