Variant report

Variant	rs73263911
Chromosome Location	chr7:14346614-14346615
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10214938	1.00[EUR][1000 genomes]
rs11975701	1.00[EUR][1000 genomes]
rs11982440	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16878125	1.00[EUR][1000 genomes]
rs73263910	0.85[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs73263942	1.00[EUR][1000 genomes]
rs73281231	1.00[EUR][1000 genomes]
rs73281248	1.00[EUR][1000 genomes]
rs73679706	1.00[EUR][1000 genomes]
rs73679719	1.00[EUR][1000 genomes]
rs7793134	1.00[EUR][1000 genomes]
rs7803632	1.00[EUR][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	nsv949033	chr7:14086106-14860323	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv606280	chr7:14327966-14352001	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:14346400-14347200	Enhancers	Fetal Heart	heart

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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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