Variant report

Variant	rs7832113
Chromosome Location	chr8:59214724-59214725
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:9)

rs_ID	r²[population]
rs16923236	1.00[AMR][1000 genomes]
rs16923298	1.00[AMR][1000 genomes]
rs16923358	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4604417	1.00[AMR][1000 genomes]
rs58710819	1.00[AMR][1000 genomes]
rs6997053	1.00[AMR][1000 genomes]
rs7820371	1.00[AMR][1000 genomes]
rs7830554	1.00[AMR][1000 genomes]
rs7839207	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	esv2761427	chr8:59204373-59242564	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:59212600-59219400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr8:59213200-59219400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr8:59213800-59215000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr8:59213800-59215000	Weak transcription	HUES64 Cell Line	embryonic stem cell

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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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