Variant report

Variant	rs7330924
Chromosome Location	chr13:95411600-95411601
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs72639821	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs72639829	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs72639833	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7993648	0.97[EUR][1000 genomes]
rs9590078	0.97[EUR][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	nsv983615	chr13:95410835-95413290	Enhancers Flanking Active TSS Weak transcription	TF binding region CpG island lncRNA	3 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	chr13:95409600-95412800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr13:95410600-95413200	Weak transcription	iPS DF 6.9 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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