Variant report

Variant	rs72948657
Chromosome Location	chr1:86202409-86202410
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs1587675	1.00[AMR][1000 genomes]
rs56845363	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57279034	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60377914	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61616564	1.00[AMR][1000 genomes]
rs6682426	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72944654	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72944667	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72944681	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72944701	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72946607	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72946610	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72946612	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72946626	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72946649	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72946658	1.00[AMR][1000 genomes]
rs72946661	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72946666	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72946671	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72946698	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72948631	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72948655	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72948683	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72948687	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72950619	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72954510	1.00[AMR][1000 genomes]
rs7517522	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1006994	chr1:85454304-86327679	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
2	esv3391173	chr1:86005637-86337469	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
3	nsv817212	chr1:86127851-86658426	Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv871471	chr1:86143084-86211516	Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:86191600-86210400	Weak transcription	Fetal Lung	lung
2	chr1:86196400-86205600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr1:86196600-86208200	Weak transcription	Primary hematopoietic stem cells	blood
4	chr1:86199000-86211600	Weak transcription	GM12878-XiMat	blood
5	chr1:86200000-86202800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr1:86202400-86209400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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