Variant report

Variant	rs72860476
Chromosome Location	chr4:78418209-78418210
allele	C/G
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]
rs72860451	0.97[AFR][1000 genomes]
rs72860458	0.86[AFR][1000 genomes]
rs72860467	0.97[AFR][1000 genomes]
rs72860468	0.97[AFR][1000 genomes]
rs72860470	0.97[AFR][1000 genomes]
rs72860477	1.00[AFR][1000 genomes]
rs72860482	1.00[AFR][1000 genomes]
rs7654195	0.94[AFR][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	esv3434529	chr4:78388030-78470631	Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription	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	chr4:78414000-78419000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr4:78415400-78424400	Weak transcription	Primary hematopoietic stem cells	blood
3	chr4:78415600-78418800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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