Variant report

Variant	rs7708703
Chromosome Location	chr5:95953260-95953261
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs72772004	0.81[EUR][1000 genomes]
rs72772009	0.81[EUR][1000 genomes]
rs72772010	0.81[EUR][1000 genomes]
rs72772014	0.81[EUR][1000 genomes]
rs72772015	0.81[EUR][1000 genomes]
rs72772019	0.81[EUR][1000 genomes]
rs72772022	0.93[EUR][1000 genomes]
rs72772023	0.93[EUR][1000 genomes]
rs72772028	0.93[EUR][1000 genomes]
rs72772031	0.93[EUR][1000 genomes]
rs72772034	0.93[EUR][1000 genomes]
rs72772036	0.93[EUR][1000 genomes]
rs72772037	0.93[EUR][1000 genomes]
rs7707773	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1030444	chr5:95353620-95995619	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
2	nsv537810	chr5:95353620-95995619	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
3	nsv1024964	chr5:95742124-96065492	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
4	nsv537811	chr5:95742124-96065492	Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
5	nsv1026484	chr5:95759910-95961518	Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:95950400-95963000	Weak transcription	Stomach Mucosa	stomach
2	chr5:95950800-95960400	Weak transcription	A549	lung
3	chr5:95951400-95961400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr5:95951400-95965000	Weak transcription	HUVEC	blood vessel
5	chr5:95952200-95964600	Weak transcription	Esophagus	oesophagus
6	chr5:95953200-95961200	Weak transcription	HMEC	breast
7	chr5:95953200-95961400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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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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