Variant report

Variant	rs1442695
Chromosome Location	chr4:78375988-78375989
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10470903	1.00[AMR][1000 genomes]
rs1604152	1.00[AMR][1000 genomes]
rs17002746	1.00[AMR][1000 genomes]
rs2165721	0.89[AFR][1000 genomes]
rs2866293	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4859500	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4859830	1.00[AMR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv829974	chr4:78240718-78415642	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:78374800-78376200	Enhancers	Fetal Lung	lung
2	chr4:78375000-78376200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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

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