Variant report

Variant	rs7727251
Chromosome Location	chr5:76272060-76272061
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10055255	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10060037	0.84[ASN][1000 genomes]
rs1053989	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1500	0.84[ASN][1000 genomes]
rs1651097	0.81[ASN][1000 genomes]
rs1651098	0.84[ASN][1000 genomes]
rs1651099	0.82[ASN][1000 genomes]
rs1651100	0.84[ASN][1000 genomes]
rs1700668	0.84[ASN][1000 genomes]
rs1715747	0.84[ASN][1000 genomes]
rs1715767	0.84[ASN][1000 genomes]
rs1715768	0.84[ASN][1000 genomes]
rs1875999	0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2135078	0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2174444	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7718461	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7721519	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7728378	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs964734	0.97[ASN][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	nsv1019669	chr5:75836365-76477788	Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
2	esv3393424	chr5:76122720-76287744	Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv1027236	chr5:76190936-76414733	Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
4	nsv830355	chr5:76194722-76368020	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
5	nsv823102	chr5:76256917-76388287	Enhancers Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 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	chr5:76260800-76275000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr5:76265800-76279000	Weak transcription	Adipose Nuclei	Adipose
3	chr5:76267800-76274800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr5:76271000-76282400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr5:76271200-76275800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr5:76271800-76275400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr5:76271800-76278400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr5:76272000-76272600	Strong transcription	Primary hematopoietic stem cells	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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