Variant report

Variant	rs9495573
Chromosome Location	chr6:140012720-140012721
allele	A/G
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:8)

rs_ID	r²[population]
rs11961450	1.00[AMR][1000 genomes]
rs11962478	1.00[AMR][1000 genomes]
rs11962747	1.00[AMR][1000 genomes]
rs11966158	1.00[AMR][1000 genomes]
rs11970015	1.00[AMR][1000 genomes]
rs6899761	1.00[AMR][1000 genomes]
rs6941139	0.85[YRI][hapmap]
rs7741203	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	nsv869066	chr6:139777114-140639695	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	26 gene(s)	inside rSNPs	diseases
2	nsv516840	chr6:139960833-140053704	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:140008200-140016000	Weak transcription	Monocytes-CD14+_RO01746	blood
2	chr6:140011600-140016000	Weak transcription	Primary monocytes fromperipheralblood	blood
3	chr6:140012200-140016800	Weak transcription	Rectal Mucosa Donor 31	rectum

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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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