Variant report

Variant	rs6947329
Chromosome Location	chr7:116943135-116943136
allele	C/T
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:13)

rs_ID	r²[population]
rs10953841	0.86[CHB][hapmap]
rs2239956	0.82[CEU][hapmap];0.95[CHB][hapmap];0.95[CHD][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs2285543	0.80[CEU][hapmap];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2285544	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.98[TSI][hapmap];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2285545	0.91[CHB][hapmap];0.89[CHD][hapmap];0.90[JPT][hapmap];0.85[TSI][hapmap];0.94[ASN][1000 genomes]
rs254536	0.86[CHB][hapmap]
rs39312	0.86[CHB][hapmap];0.84[CHD][hapmap]
rs39315	0.86[CHB][hapmap]
rs39317	0.86[CHB][hapmap]
rs39324	0.86[CHB][hapmap]
rs4727848	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6946481	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs739517	0.86[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831108	chr7:116749534-116952011	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
2	nsv608256	chr7:116928371-117040117	Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:116920400-116943800	Weak transcription	Right Atrium	heart
2	chr7:116931800-116961600	Weak transcription	Placenta	Placenta
3	chr7:116936400-116952200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr7:116937000-116954800	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr7:116941600-116943800	Weak transcription	Fetal Lung	lung

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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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