Variant report

Variant	rs7757369
Chromosome Location	chr6:147158541-147158542
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs6940979	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73789013	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7760389	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9485127	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9497642	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9497645	0.98[AFR][1000 genomes]
rs9497648	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9497662	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	nsv830838	chr6:147090745-147274669	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:147150200-147162200	Weak transcription	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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