Variant report

Variant	rs73417767
Chromosome Location	chr15:54678868-54678869
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs61086197	0.91[AFR][1000 genomes]
rs73415703	0.83[AFR][1000 genomes]
rs73415705	0.83[AFR][1000 genomes]
rs73415710	0.83[AFR][1000 genomes]
rs73415711	0.83[AFR][1000 genomes]
rs73415722	0.83[AFR][1000 genomes]
rs73415723	0.83[AFR][1000 genomes]
rs73415738	0.83[AFR][1000 genomes]
rs73415762	0.83[AFR][1000 genomes]
rs73417711	0.91[AFR][1000 genomes]
rs73417732	0.91[AFR][1000 genomes]
rs73417771	1.00[AFR][1000 genomes]
rs73417779	0.96[AFR][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	nsv817539	chr15:54132584-55095235	Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	esv1845471	chr15:54556063-54685463	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr15:54678800-54679000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr15:54678800-54679400	Flanking Active TSS	Aorta	Aorta

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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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