Variant report

Variant	rs6960352
Chromosome Location	chr7:21876008-21876009
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10225993	1.00[CEU][hapmap];0.81[YRI][hapmap];1.00[EUR][1000 genomes]
rs10267329	1.00[EUR][1000 genomes]
rs11972036	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs11972218	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs11973100	1.00[CEU][hapmap];0.91[YRI][hapmap];0.88[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs6461606	1.00[CEU][hapmap];0.95[YRI][hapmap];0.88[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs6461607	1.00[EUR][1000 genomes]
rs6461615	1.00[CEU][hapmap]
rs6960272	0.98[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs6960422	0.98[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73277785	0.93[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73277786	0.99[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7783482	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs7799414	1.00[EUR][1000 genomes]
rs7800783	1.00[MEX][hapmap]
rs7807695	1.00[ASW][hapmap];0.89[MKK][hapmap];0.87[YRI][hapmap];0.86[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1018133	chr7:21740118-22055283	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
2	nsv830922	chr7:21793386-21964675	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	3 gene(s)	inside rSNPs	diseases
3	nsv933320	chr7:21840543-21882825	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv2761158	chr7:21863894-21877962	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:21860400-21882200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr7:21869800-21884400	Weak transcription	Cortex derived primary cultured neurospheres	brain

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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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