Variant report

Variant	rs72915665
Chromosome Location	chr3:88006236-88006237
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs72913747	1.00[AFR][1000 genomes]
rs72913758	1.00[AFR][1000 genomes]
rs72913780	1.00[AFR][1000 genomes]
rs72915611	1.00[AFR][1000 genomes]
rs72915637	1.00[AFR][1000 genomes]
rs72915646	1.00[AFR][1000 genomes]
rs72915662	1.00[AFR][1000 genomes]
rs72915670	1.00[AFR][1000 genomes]
rs72915677	1.00[AFR][1000 genomes]
rs72915684	1.00[AFR][1000 genomes]
rs72915697	1.00[AFR][1000 genomes]
rs72917717	1.00[AFR][1000 genomes]
rs72917722	0.89[AFR][1000 genomes]
rs72917736	0.89[AFR][1000 genomes]
rs72917744	0.89[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	nsv834758	chr3:87867363-88014975	Strong transcription Enhancers ZNF genes & repeats Weak transcription Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv877146	chr3:87983962-88159835	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	12 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	chr3:87995600-88011000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr3:88005000-88011200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr3:88006200-88008200	Strong transcription	Primary hematopoietic stem cells	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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