Variant report

Variant	rs1792627
Chromosome Location	chr11:94079436-94079437
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs4301753	1.00[AMR][1000 genomes]
rs505417	1.00[AMR][1000 genomes]
rs511184	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs532108	1.00[AMR][1000 genomes]
rs585441	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs608452	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6483328	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6483330	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6483333	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7101762	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7120020	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv523083	chr11:93962121-94150790	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
2	nsv832233	chr11:93981434-94158471	Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 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	chr11:94077600-94079800	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr11:94079400-94079800	Weak transcription	iPS-18 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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