Variant report

Variant	rs10470827
Chromosome Location	chr4:28007853-28007854
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs11932457	0.92[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs11939735	0.92[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs16880102	0.89[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs2192545	0.92[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs28520329	0.89[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs9993475	0.92[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs9999672	0.89[AFR][1000 genomes];0.85[AMR][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	nsv1013877	chr4:27539626-28051576	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1007066	chr4:28001862-28131764	Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv878772	chr4:28006005-28030505	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:28006000-28012400	Weak transcription	Brain Cingulate Gyrus	brain
2	chr4:28006400-28009200	Weak transcription	Brain Anterior Caudate	brain
3	chr4:28006600-28009400	Weak transcription	Brain Hippocampus Middle	brain
4	chr4:28007600-28008600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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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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