Variant report

Variant	rs7804932
Chromosome Location	chr7:78112280-78112281
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10156060	0.83[YRI][hapmap]
rs11973630	0.95[EUR][1000 genomes]
rs11977168	0.86[CEU][hapmap];0.95[EUR][1000 genomes]
rs11977779	0.82[CEU][hapmap];0.94[EUR][1000 genomes]
rs12667712	0.91[CEU][hapmap];0.95[EUR][1000 genomes]
rs1548868	0.96[YRI][hapmap];0.85[AFR][1000 genomes]
rs1990577	0.96[YRI][hapmap];0.84[AFR][1000 genomes]
rs2192646	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2192647	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2215933	0.89[EUR][1000 genomes]
rs2362610	0.94[EUR][1000 genomes]
rs34403226	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs35454028	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3735442	0.96[YRI][hapmap];0.85[AFR][1000 genomes]
rs4996259	0.90[YRI][hapmap]
rs6466243	0.86[CEU][hapmap];0.95[EUR][1000 genomes]
rs67578259	0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6950700	0.90[EUR][1000 genomes]
rs6951193	0.92[CEU][hapmap];0.94[EUR][1000 genomes]
rs7780645	0.83[CEU][hapmap];0.95[EUR][1000 genomes]
rs7780794	0.91[CEU][hapmap];0.95[EUR][1000 genomes]
rs7784056	0.90[YRI][hapmap]
rs7784896	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7804602	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7804616	0.80[CEU][hapmap]
rs9640709	0.91[CEU][hapmap];0.95[EUR][1000 genomes]
rs9641412	0.92[CEU][hapmap];0.95[EUR][1000 genomes]
rs972544	0.95[EUR][1000 genomes]
rs974346	0.95[EUR][1000 genomes]
rs974347	0.94[EUR][1000 genomes]
rs975421	0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][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	nsv1022764	chr7:77911072-78316607	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1022199	chr7:78054639-78469370	Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv538986	chr7:78054639-78469370	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:78103000-78117600	Weak transcription	Fetal Brain Female	brain
2	chr7:78103800-78115600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr7:78104400-78116800	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr7:78105600-78113800	Weak transcription	Brain Hippocampus Middle	brain
5	chr7:78106200-78113200	Weak transcription	Brain Anterior Caudate	brain
6	chr7:78106400-78113600	Weak transcription	Brain Substantia Nigra	brain
7	chr7:78106600-78114000	Weak transcription	Brain Cingulate Gyrus	brain
8	chr7:78106600-78117000	Weak transcription	Brain Germinal Matrix	brain
9	chr7:78108400-78116800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr7:78108800-78117400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr7:78108800-78118800	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr7:78109000-78118200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr7:78109200-78114400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr7:78109600-78117600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr7:78109600-78118600	Weak transcription	Fetal Heart	heart

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