Variant report

Variant	rs10256755
Chromosome Location	chr7:21881118-21881119
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs11975573	0.81[YRI][hapmap];1.00[EUR][1000 genomes]
rs11976836	1.00[EUR][1000 genomes]
rs17145131	1.00[EUR][1000 genomes]
rs17145187	1.00[EUR][1000 genomes]
rs17145195	1.00[EUR][1000 genomes]
rs17145222	1.00[EUR][1000 genomes]
rs28415111	1.00[EUR][1000 genomes]
rs6960910	1.00[EUR][1000 genomes]
rs73275610	1.00[EUR][1000 genomes]
rs73275617	1.00[EUR][1000 genomes]
rs73275618	1.00[EUR][1000 genomes]
rs9969170	1.00[EUR][1000 genomes]
rs9969255	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 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

No data

Chromatin state (count:4 , 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
3	chr7:21881000-21881200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr7:21881000-21881200	Enhancers	Pancreas	Pancrea

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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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