Variant report

Variant	rs6968769
Chromosome Location	chr7:41103473-41103474
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs10244205	0.99[ASN][1000 genomes]
rs11765348	0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11974873	0.89[ASN][1000 genomes]
rs12673561	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs13236299	0.87[ASN][1000 genomes]
rs1859702	0.99[ASN][1000 genomes]
rs2190345	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][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	nsv1034605	chr7:41096638-41222426	Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:41098600-41104600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr7:41099200-41104800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr7:41099600-41104800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr7:41100000-41104600	Weak transcription	HMEC	breast
5	chr7:41101000-41113000	Weak transcription	Aorta	Aorta
6	chr7:41101000-41117800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr7:41102600-41103800	Enhancers	Primary neutrophils fromperipheralblood	blood

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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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