Variant report

Variant	rs73120656
Chromosome Location	chr1:239741583-239741584
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs12080179	0.89[ASN][1000 genomes]
rs55810060	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs60623103	0.83[ASN][1000 genomes]
rs67065820	0.84[ASN][1000 genomes]
rs67802170	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs67920721	0.83[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs67978876	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73116727	0.93[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs73120637	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73120645	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73120652	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73120655	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73120657	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73120670	0.94[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs73122635	0.94[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs73122647	0.94[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs73122651	0.93[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs73122654	0.81[AMR][1000 genomes]
rs73122657	0.81[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	nsv1002301	chr1:239182255-239774393	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv549435	chr1:239375010-239974006	Active TSS Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	esv3377526	chr1:239623743-240111639	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
4	nsv873351	chr1:239636613-240324200	Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 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	chr1:239728800-239769400	Weak transcription	Primary hematopoietic stem cells	blood
2	chr1:239735000-239746600	Weak transcription	Ovary	ovary
3	chr1:239735200-239745800	Weak transcription	Pancreas	Pancrea
4	chr1:239738800-239748600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr1:239739000-239745600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr1:239739000-239748600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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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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