Variant report

Variant	rs61334019
Chromosome Location	chr12:44853255-44853256
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10467198	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11182492	0.87[AFR][1000 genomes]
rs11182494	0.87[AFR][1000 genomes]
rs11182503	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12300006	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12301186	1.00[AMR][1000 genomes]
rs12304363	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12308192	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12310486	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12311300	1.00[AMR][1000 genomes]
rs12322750	1.00[AMR][1000 genomes]
rs1493753	0.80[AFR][1000 genomes]
rs1493757	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56009337	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57316311	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59907388	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60037016	1.00[AMR][1000 genomes]
rs60810059	1.00[AMR][1000 genomes]
rs74085006	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74085037	1.00[AMR][1000 genomes]
rs74085043	1.00[AMR][1000 genomes]
rs74085152	1.00[AMR][1000 genomes]
rs74087530	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9971775	0.90[AFR][1000 genomes];1.00[AMR][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	nsv1049818	chr12:44486312-45133783	Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:44851800-44857400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr12:44852200-44857200	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr12:44852200-44859600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr12:44852800-44853600	Enhancers	Fetal Brain Male	brain

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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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